Primary Site >> Stomach Cancer
Gene >> SYNE1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152242367:152242367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.19766G>C |
| AA Mutation | p.Ser6589Thr(p.S6589T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152321362:152321362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs527462104 |
| CDS Mutation | c.16112G>A |
| AA Mutation | p.Arg5371Gln(p.R5371Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152444518:152444518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3730T>A |
| AA Mutation | p.Ser1244Thr(p.S1244T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152520527:152520527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375917264 |
| CDS Mutation | c.241C>T |
| AA Mutation | p.Arg81Cys(p.R81C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152318972:152318972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.16280G>T |
| AA Mutation | p.Ser5427Ile(p.S5427I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152318106:152318106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.16547A>G |
| AA Mutation | p.Glu5516Gly(p.E5516G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152331441:152331441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13244T>G |
| AA Mutation | p.Leu4415Arg(p.L4415R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152455529:152455529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2789A>C |
| AA Mutation | p.Lys930Thr(p.K930T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152236297:152236297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.20206A>C |
| AA Mutation | p.Lys6736Gln(p.K6736Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152242383:152242383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.19750A>T |
| AA Mutation | p.Asn6584Tyr(p.N6584Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152401243:152401243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6924A>C |
| AA Mutation | p.Gln2308His(p.Q2308H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152334120:152334120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12682C>A |
| AA Mutation | p.Leu4228Met(p.L4228M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152330262:152330262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373040273 |
| CDS Mutation | c.14423C>T |
| AA Mutation | p.Thr4808Met(p.T4808M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152364946:152364946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10046A>C |
| AA Mutation | p.Gln3349Pro(p.Q3349P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152350624:152350624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367946740 |
| CDS Mutation | c.11727A>G |
| AA Mutation | p.Ile3909Met(p.I3909M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152230567:152230567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.21175A>C |
| AA Mutation | p.Asn7059His(p.N7059H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152350223:152350223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11846A>G |
| AA Mutation | p.Asp3949Gly(p.D3949G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152141250:152141250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769976238 |
| CDS Mutation | c.25199G>T |
| AA Mutation | p.Ser8400Ile(p.S8400I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152143735:152143735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200684943 |
| CDS Mutation | c.25007G>A |
| AA Mutation | p.Arg8336Gln(p.R8336Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152455902:152455902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2711T>C |
| AA Mutation | p.Ile904Thr(p.I904T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152367322:152367322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9868A>C |
| AA Mutation | p.Lys3290Gln(p.K3290Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152376855:152376855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9067C>A |
| AA Mutation | p.Leu3023Met(p.L3023M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152325112:152325112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15629T>A |
| AA Mutation | p.Val5210Glu(p.V5210E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152329740:152329740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754495941 |
| CDS Mutation | c.14945G>A |
| AA Mutation | p.Arg4982His(p.R4982H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152387253:152387253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8306A>C |
| AA Mutation | p.Lys2769Thr(p.K2769T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152416850:152416850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769949513 |
| CDS Mutation | c.5587C>T |
| AA Mutation | p.Arg1863Trp(p.R1863W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152164199:152164199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546350017 |
| CDS Mutation | c.23754C>G |
| AA Mutation | p.Asn7918Lys(p.N7918K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152330546:152330546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14139A>C |
| AA Mutation | p.Gln4713His(p.Q4713H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152321318:152321318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.16156T>G |
| AA Mutation | p.Leu5386Val(p.L5386V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152323548:152323548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.15847G>A |
| AA Mutation | p.Ala5283Thr(p.A5283T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152325160:152325160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751121212 |
| CDS Mutation | c.15581G>A |
| AA Mutation | p.Arg5194His(p.R5194H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152331463:152331463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368709678 |
| CDS Mutation | c.13222G>A |
| AA Mutation | p.Ala4408Thr(p.A4408T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152381192:152381192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8823G>T |
| AA Mutation | p.Gln2941His(p.Q2941H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152455467:152455467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2851G>A |
| AA Mutation | p.Glu951Lys(p.E951K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152430503:152430503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774194598 |
| CDS Mutation | c.4668G>C |
| AA Mutation | p.Lys1556Asn(p.K1556N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152230641:152230641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.21101T>A |
| AA Mutation | p.Leu7034Gln(p.L7034Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152352178:152352178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375577011 |
| CDS Mutation | c.11429C>T |
| AA Mutation | p.Thr3810Met(p.T3810M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152358507:152358507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs531503159 |
| CDS Mutation | c.10474C>T |
| AA Mutation | p.Arg3492Cys(p.R3492C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152151988:152151988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200118773 |
| CDS Mutation | c.24283C>T |
| AA Mutation | p.Arg8095Cys(p.R8095C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152520487:152520487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746029148 |
| CDS Mutation | c.281C>T |
| AA Mutation | p.Thr94Met(p.T94M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367255 |
| Start | 152331888:152331888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12797C>T |
| AA Mutation | p.Ser4266Phe(p.S4266F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152220990:152220990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.21713T>G |
| AA Mutation | p.Leu7238Arg(p.L7238R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152148088:152148088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.24933G>T |
| AA Mutation | p.Gln8311His(p.Q8311H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152254999:152254999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755740366 |
| CDS Mutation | c.19351C>G |
| AA Mutation | p.Arg6451Gly(p.R6451G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152310734:152310734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141550859 |
| CDS Mutation | c.16850G>A |
| AA Mutation | p.Arg5617Gln(p.R5617Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152471751:152471751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1478C>T |
| AA Mutation | p.Ser493Phe(p.S493F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152505323:152505323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.656C>T |
| AA Mutation | p.Ala219Val(p.A219V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152425533:152425533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5115A>C |
| AA Mutation | p.Glu1705Asp(p.E1705D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152329762:152329762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14923G>A |
| AA Mutation | p.Gly4975Arg(p.G4975R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152391497:152391497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7784G>T |
| AA Mutation | p.Gly2595Val(p.G2595V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152520524:152520524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772761179 |
| CDS Mutation | c.244C>T |
| AA Mutation | p.Arg82Trp(p.R82W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152354816:152354816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762304790 |
| CDS Mutation | c.10769G>A |
| AA Mutation | p.Arg3590Gln(p.R3590Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152164266:152164266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.23687G>T |
| AA Mutation | p.Ser7896Ile(p.S7896I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152208150:152208150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201841732 |
| CDS Mutation | c.22646G>A |
| AA Mutation | p.Arg7549His(p.R7549H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152416612:152416612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5825C>A |
| AA Mutation | p.Ser1942Tyr(p.S1942Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152428374:152428374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4807G>A |
| AA Mutation | p.Glu1603Lys(p.E1603K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152441194:152441194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768987820 |
| CDS Mutation | c.4085G>T |
| AA Mutation | p.Ser1362Ile(p.S1362I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152442232:152442232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779032686 |
| CDS Mutation | c.3851G>A |
| AA Mutation | p.Arg1284Gln(p.R1284Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152330605:152330605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14080T>A |
| AA Mutation | p.Phe4694Ile(p.F4694I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152219025:152219025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.22022G>A |
| AA Mutation | p.Cys7341Tyr(p.C7341Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152301976:152301976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775815795 |
| CDS Mutation | c.17434G>A |
| AA Mutation | p.Ala5812Thr(p.A5812T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152239567:152239567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768271480 |
| CDS Mutation | c.20033A>C |
| AA Mutation | p.His6678Pro(p.H6678P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152483098:152483098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1337T>C |
| AA Mutation | p.Leu446Pro(p.L446P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152132199:152132199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.26017T>A |
| AA Mutation | p.Ser8673Thr(p.S8673T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152151969:152151969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748375969 |
| CDS Mutation | c.24302G>A |
| AA Mutation | p.Arg8101His(p.R8101H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152331807:152331807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12878A>G |
| AA Mutation | p.Glu4293Gly(p.E4293G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 67 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152156025:152156025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.23863C>T |
| AA Mutation | p.His7955Tyr(p.H7955Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 68 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152221551:152221551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.21531A>C |
| AA Mutation | p.Gln7177His(p.Q7177H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 69 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152362240:152362240(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10229C>T |
| AA Mutation | p.Ala3410Val(p.A3410V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 70 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152208081:152208081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.22715C>T |
| AA Mutation | p.Ala7572Val(p.A7572V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 71 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152293710:152293710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748231030 |
| CDS Mutation | c.17890C>T |
| AA Mutation | p.Arg5964Cys(p.R5964C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 72 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152331571:152331571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13114A>G |
| AA Mutation | p.Lys4372Glu(p.K4372E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 73 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152369097:152369097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9682C>T |
| AA Mutation | p.Pro3228Ser(p.P3228S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 74 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152396944:152396944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7387C>A |
| AA Mutation | p.Leu2463Ile(p.L2463I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 75 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152455971:152455971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2642A>T |
| AA Mutation | p.Lys881Met(p.K881M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 76 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152483098:152483098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1337T>G |
| AA Mutation | p.Leu446Arg(p.L446R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 77 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152323518:152323518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15877C>G |
| AA Mutation | p.Leu5293Val(p.L5293V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 78 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152242347:152242347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.19786C>G |
| AA Mutation | p.Gln6596Glu(p.Q6596E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 79 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152390287:152390287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547324404 |
| CDS Mutation | c.8170G>A |
| AA Mutation | p.Ala2724Thr(p.A2724T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 80 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152331873:152331873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12812C>T |
| AA Mutation | p.Thr4271Ile(p.T4271I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 81 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367255 |
| Start | 152249163:152249163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.19570G>C |
| AA Mutation | p.Glu6524Gln(p.E6524Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 82 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152444433:152444433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3815A>C |
| AA Mutation | p.Gln1272Pro(p.Q1272P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 83 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152164294:152164294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143842011 |
| CDS Mutation | c.23659G>A |
| AA Mutation | p.Val7887Met(p.V7887M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 84 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152329816:152329816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14869G>A |
| AA Mutation | p.Glu4957Lys(p.E4957K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 85 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152488498:152488498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.945A>C |
| AA Mutation | p.Glu315Asp(p.E315D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 86 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152461656:152461656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2335C>G |
| AA Mutation | p.Gln779Glu(p.Q779E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 87 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152164266:152164266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.23687G>A |
| AA Mutation | p.Ser7896Asn(p.S7896N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 88 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152334237:152334237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148204741 |
| CDS Mutation | c.12565G>A |
| AA Mutation | p.Val4189Met(p.V4189M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 89 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152453630:152453630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2983C>A |
| AA Mutation | p.Gln995Lys(p.Q995K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 90 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152398647:152398647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7322T>G |
| AA Mutation | p.Val2441Gly(p.V2441G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 91 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152359379:152359379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750619051 |
| CDS Mutation | c.10379A>G |
| AA Mutation | p.Tyr3460Cys(p.Y3460C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 92 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152428253:152428253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753598584 |
| CDS Mutation | c.4928C>T |
| AA Mutation | p.Ala1643Val(p.A1643V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 93 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152334150:152334150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12652T>G |
| AA Mutation | p.Trp4218Gly(p.W4218G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 94 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152350253:152350253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11816T>C |
| AA Mutation | p.Leu3939Pro(p.L3939P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 95 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152350309:152350309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11760A>C |
| AA Mutation | p.Lys3920Asn(p.K3920N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 96 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152354931:152354931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10654G>A |
| AA Mutation | p.Val3552Met(p.V3552M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 97 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152234747:152234747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201037542 |
| CDS Mutation | c.20450G>A |
| AA Mutation | p.Arg6817Gln(p.R6817Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 98 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152352193:152352193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11414G>A |
| AA Mutation | p.Arg3805Gln(p.R3805Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 99 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152242341:152242341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.19792C>A |
| AA Mutation | p.Leu6598Met(p.L6598M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 100 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152310491:152310491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.16924A>C |
| AA Mutation | p.Lys5642Gln(p.K5642Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 101 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152350324:152350324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11745C>A |
| AA Mutation | p.Phe3915Leu(p.F3915L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 102 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152326591:152326591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14998C>G |
| AA Mutation | p.Gln5000Glu(p.Q5000E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 103 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152325200:152325200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15541C>A |
| AA Mutation | p.Leu5181Met(p.L5181M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 104 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152339279:152339279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12313A>G |
| AA Mutation | p.Lys4105Glu(p.K4105E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 105 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152347163:152347163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11974G>T |
| AA Mutation | p.Gly3992Cys(p.G3992C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 106 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152353297:152353297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11219C>T |
| AA Mutation | p.Thr3740Ile(p.T3740I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 107 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152284091:152284091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.18094T>C |
| AA Mutation | p.Ser6032Pro(p.S6032P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 108 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152224498:152224498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.21518T>G |
| AA Mutation | p.Leu7173Arg(p.L7173R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 109 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152505248:152505248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.731C>G |
| AA Mutation | p.Thr244Ser(p.T244S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 110 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152213653:152213653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.22453G>A |
| AA Mutation | p.Gly7485Arg(p.G7485R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 111 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152483105:152483105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs75153800 |
| CDS Mutation | c.1330C>T |
| AA Mutation | p.Arg444Trp(p.R444W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 112 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152331130:152331130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571224180 |
| CDS Mutation | c.13555G>A |
| AA Mutation | p.Glu4519Lys(p.E4519K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 113 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152132169:152132169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.26047T>C |
| AA Mutation | p.Ser8683Pro(p.S8683P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 114 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152462809:152462809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2179G>A |
| AA Mutation | p.Ala727Thr(p.A727T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 115 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152318157:152318157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.16496A>T |
| AA Mutation | p.Lys5499Met(p.K5499M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 116 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152148287:152148287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.24734C>T |
| AA Mutation | p.Ala8245Val(p.A8245V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 117 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152331085:152331085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13600G>A |
| AA Mutation | p.Gly4534Arg(p.G4534R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 118 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152376842:152376842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9080G>T |
| AA Mutation | p.Cys3027Phe(p.C3027F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 119 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152396943:152396943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7388T>A |
| AA Mutation | p.Leu2463His(p.L2463H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 120 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152391494:152391494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7787G>A |
| AA Mutation | p.Arg2596His(p.R2596H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 121 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152526150:152526150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.155A>G |
| AA Mutation | p.Asp52Gly(p.D52G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 122 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152221469:152221469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377449974 |
| CDS Mutation | c.21613G>A |
| AA Mutation | p.Val7205Met(p.V7205M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 123 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152318157:152318157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.16496A>C |
| AA Mutation | p.Lys5499Thr(p.K5499T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 124 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152281974:152281974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.18214T>G |
| AA Mutation | p.Leu6072Val(p.L6072V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 125 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152396894:152396894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7437A>C |
| AA Mutation | p.Lys2479Asn(p.K2479N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 126 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152133326:152133326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149045775 |
| CDS Mutation | c.25951C>T |
| AA Mutation | p.Arg8651Cys(p.R8651C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 127 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152510311:152510311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774342833 |
| CDS Mutation | c.463G>A |
| AA Mutation | p.Val155Met(p.V155M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 128 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152350223:152350223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11846A>T |
| AA Mutation | p.Asp3949Val(p.D3949V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 129 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152396847:152396847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7484A>G |
| AA Mutation | p.Glu2495Gly(p.E2495G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 130 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152330826:152330826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13859T>G |
| AA Mutation | p.Leu4620Arg(p.L4620R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 131 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152350294:152350294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11775A>C |
| AA Mutation | p.Glu3925Asp(p.E3925D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 132 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152505290:152505290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.689T>C |
| AA Mutation | p.Val230Ala(p.V230A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 133 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152413417:152413417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6165A>C |
| AA Mutation | p.Glu2055Asp(p.E2055D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 134 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152151656:152151656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781159250 |
| CDS Mutation | c.24347C>T |
| AA Mutation | p.Ala8116Val(p.A8116V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 135 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152239640:152239640(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.19960T>C |
| AA Mutation | p.Phe6654Leu(p.F6654L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 136 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367255 |
| Start | 152425381:152425381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5267G>A |
| AA Mutation | p.Arg1756Lys(p.R1756K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 137 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152520485:152520485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.283G>A |
| AA Mutation | p.Ala95Thr(p.A95T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 138 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152331131:152331131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115535983 |
| CDS Mutation | c.13554C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 139 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152404249:152404249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6789A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 140 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152330579:152330579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146180064 |
| CDS Mutation | c.14106C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 141 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152269206:152269206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.18654A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 142 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152219123:152219123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371017408 |
| CDS Mutation | c.21924G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 143 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152395608:152395608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142663488 |
| CDS Mutation | c.7620G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 144 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152213690:152213690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.22416A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 145 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152330570:152330570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377739292 |
| CDS Mutation | c.14115C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 146 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152391412:152391412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7869T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 147 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152206252:152206252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369873269 |
| CDS Mutation | c.22935C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 148 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152451161:152451161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3072T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 149 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152362269:152362269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10200G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 150 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152330651:152330651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14034C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 151 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152404290:152404290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6748A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 152 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152294053:152294053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550385131 |
| CDS Mutation | c.17757C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 153 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152344156:152344156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12150C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 154 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152369567:152369567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9555C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 155 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152236883:152236883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.20133C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 156 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152278095:152278095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.18567C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 157 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152239683:152239683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.19917T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 158 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152301947:152301947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.17463C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 159 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152390288:152390288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371449580 |
| CDS Mutation | c.8169C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 160 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152428234:152428234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771626624 |
| CDS Mutation | c.4947G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 161 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152148235:152148235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.24786T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 162 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152350240:152350240(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146547806 |
| CDS Mutation | c.11829C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 163 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152336886:152336886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12483T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 164 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152483178:152483178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1257C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 165 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152369002:152369002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9777T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 166 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152221533:152221533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.21549G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 167 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152309940:152309940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769890058 |
| CDS Mutation | c.17097C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 168 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152461687:152461687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2304G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 169 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152293642:152293642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.17958C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 170 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152122616:152122616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529628600 |
| CDS Mutation | c.26214C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 171 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152326622:152326622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14967T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 172 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152387156:152387156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757104773 |
| CDS Mutation | c.8403C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 173 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152164289:152164289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375008462 |
| CDS Mutation | c.23664G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 174 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152331215:152331215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13470C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 175 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152269185:152269185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373495185 |
| CDS Mutation | c.18675G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 176 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152336892:152336892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12477G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 177 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152330380:152330380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14305A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 178 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152236238:152236238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.20265A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 179 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152396930:152396930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7401T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 180 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152526113:152526113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.192T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 181 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152413447:152413447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6135T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 182 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152416599:152416599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5838T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 183 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152461672:152461672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2319T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 184 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152283999:152283999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.18186G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 185 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152206339:152206339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.22848G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 186 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152362188:152362188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147402839 |
| CDS Mutation | c.10281G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 187 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152331458:152331458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13227C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 188 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152310799:152310799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142010074 |
| CDS Mutation | c.16785C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 189 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367255 |
| Start | 152430641:152430641(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4530delT |
| AA Mutation | p.Phe1510LeufsTer17(p.F1510Lfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 190 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367255 |
| Start | 152350665:152350665(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.11686delA |
| AA Mutation | p.Ile3896Ter(p.I3896*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 191 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367255 |
| Start | 152387293:152387293(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.8266delA |
| AA Mutation | p.Ile2756Ter(p.I2756*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 192 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367255 |
| Start | 152135107:152135107(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.25785delT |
| AA Mutation | p.Met8596CysfsTer3(p.M8596Cfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 193 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367255 |
| Start | 152458772:152458772(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2553delT |
| AA Mutation | p.Phe851LeufsTer9(p.F851Lfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 194 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367255 |
| Start | 152330291:152330291(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.14394delA |
| AA Mutation | p.Glu4799ArgfsTer6(p.E4799Rfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 195 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367255 |
| Start | 152352048:152352048(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.11559delA |
| AA Mutation | p.Ala3854LeufsTer20(p.A3854Lfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 196 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367255 |
| Start | 152213742:152213742(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.22364delT |
| AA Mutation | p.Leu7455CysfsTer18(p.L7455Cfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 197 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367255 |
| Start | 152416494:152416494(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5943delA |
| AA Mutation | p.Ala1982HisfsTer10(p.A1982Hfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 198 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000367255 |
| Start | 152300643:152300643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.17680C>T |
| AA Mutation | p.Gln5894Ter(p.Q5894*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 199 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000367255 |
| Start | 152416886:152416886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5551C>T |
| AA Mutation | p.Gln1851Ter(p.Q1851*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 200 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000367255 |
| Start | 152140078:152140078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.25330C>T |
| AA Mutation | p.Gln8444Ter(p.Q8444*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 201 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000367255 |
| Start | 152242365:152242365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.19768C>T |
| AA Mutation | p.Gln6590Ter(p.Q6590*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 202 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000367255 |
| Start | 152330566:152330566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14119G>T |
| AA Mutation | p.Glu4707Ter(p.E4707*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 203 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000367255 |
| Start | 152416565:152416565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5872G>T |
| AA Mutation | p.Glu1958Ter(p.E1958*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 204 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000367255 |
| Start | 152310735:152310735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758379604 |
| CDS Mutation | c.16849C>T |
| AA Mutation | p.Arg5617Ter(p.R5617*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 205 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000367255 |
| Start | 152155026:152155026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570916267 |
| CDS Mutation | c.23995C>T |
| AA Mutation | p.Arg7999Ter(p.R7999*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |