Primary Site >> Stomach Cancer
Gene >> FCGBP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39894062:39894062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5699G>C |
| AA Mutation | p.Ser1900Thr(p.S1900T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39875465:39875465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10526C>A |
| AA Mutation | p.Pro3509His(p.P3509H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39892033:39892033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6610G>A |
| AA Mutation | p.Ala2204Thr(p.A2204T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39886329:39886329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7850G>A |
| AA Mutation | p.Gly2617Asp(p.G2617D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39873757:39873757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148917660 |
| CDS Mutation | c.10642G>A |
| AA Mutation | p.Gly3548Ser(p.G3548S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39863679:39863679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12547C>T |
| AA Mutation | p.His4183Tyr(p.H4183Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39891970:39891970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6673G>A |
| AA Mutation | p.Val2225Met(p.V2225M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39928042:39928042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201635572 |
| CDS Mutation | c.320C>T |
| AA Mutation | p.Ala107Val(p.A107V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39918332:39918332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1964A>C |
| AA Mutation | p.Asn655Thr(p.N655T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39928094:39928094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.268G>A |
| AA Mutation | p.Val90Ile(p.V90I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39875709:39875709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745724423 |
| CDS Mutation | c.10282G>A |
| AA Mutation | p.Gly3428Arg(p.G3428R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39899603:39899603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4880G>A |
| AA Mutation | p.Gly1627Glu(p.G1627E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39915397:39915397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2617G>A |
| AA Mutation | p.Val873Met(p.V873M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39891955:39891955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6688G>T |
| AA Mutation | p.Ala2230Ser(p.A2230S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39901972:39901972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4738G>A |
| AA Mutation | p.Val1580Met(p.V1580M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39879598:39879598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8825G>A |
| AA Mutation | p.Gly2942Asp(p.G2942D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39886075:39886075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8104C>T |
| AA Mutation | p.Leu2702Phe(p.L2702F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39886196:39886196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7983C>A |
| AA Mutation | p.Phe2661Leu(p.F2661L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39902327:39902327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4501C>T |
| AA Mutation | p.Leu1501Phe(p.L1501F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39902448:39902448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4380C>A |
| AA Mutation | p.Phe1460Leu(p.F1460L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000616721 |
| Start | 39875388:39875388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs537526940 |
| CDS Mutation | c.10603C>T |
| AA Mutation | p.Pro3535Ser(p.P3535S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39902018:39902018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4692G>T |
| AA Mutation | p.Glu1564Asp(p.E1564D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39924496:39924496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1540G>A |
| AA Mutation | p.Glu514Lys(p.E514K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39872293:39872293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11534G>A |
| AA Mutation | p.Ser3845Asn(p.S3845N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39918530:39918530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1766A>G |
| AA Mutation | p.Tyr589Cys(p.Y589C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39928078:39928078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.284A>G |
| AA Mutation | p.Lys95Arg(p.K95R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39878013:39878013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9092A>G |
| AA Mutation | p.Asn3031Ser(p.N3031S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39870334:39870334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184463001 |
| CDS Mutation | c.11831C>T |
| AA Mutation | p.Thr3944Met(p.T3944M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39872269:39872269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201686360 |
| CDS Mutation | c.11558G>A |
| AA Mutation | p.Arg3853Gln(p.R3853Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39870374:39870374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11791C>G |
| AA Mutation | p.Arg3931Gly(p.R3931G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39891649:39891649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6994T>G |
| AA Mutation | p.Phe2332Val(p.F2332V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39886095:39886095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8084G>A |
| AA Mutation | p.Gly2695Asp(p.G2695D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39927938:39927938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.424G>A |
| AA Mutation | p.Glu142Lys(p.E142K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39902522:39902522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4306C>T |
| AA Mutation | p.Pro1436Ser(p.P1436S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39875828:39875828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10163T>C |
| AA Mutation | p.Leu3388Pro(p.L3388P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39894186:39894186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5575G>C |
| AA Mutation | p.Gly1859Arg(p.G1859R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39892041:39892041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762633802 |
| CDS Mutation | c.6602C>T |
| AA Mutation | p.Ala2201Val(p.A2201V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39873511:39873511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762789511 |
| CDS Mutation | c.10888G>A |
| AA Mutation | p.Ala3630Thr(p.A3630T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39902521:39902521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139250740 |
| CDS Mutation | c.4307C>T |
| AA Mutation | p.Pro1436Leu(p.P1436L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39928303:39928303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751978881 |
| CDS Mutation | c.59T>C |
| AA Mutation | p.Leu20Ser(p.L20S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39891691:39891691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6952C>G |
| AA Mutation | p.Gln2318Glu(p.Q2318E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39913980:39913980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751928200 |
| CDS Mutation | c.3107C>T |
| AA Mutation | p.Thr1036Met(p.T1036M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39875727:39875727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10264G>A |
| AA Mutation | p.Asp3422Asn(p.D3422N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39915486:39915486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2528C>T |
| AA Mutation | p.Ala843Val(p.A843V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39927786:39927786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.576A>T |
| AA Mutation | p.Arg192Ser(p.R192S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39872416:39872416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775275649 |
| CDS Mutation | c.11411C>T |
| AA Mutation | p.Ala3804Val(p.A3804V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39913850:39913850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3237T>G |
| AA Mutation | p.His1079Gln(p.H1079Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39892934:39892934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6433G>C |
| AA Mutation | p.Ala2145Pro(p.A2145P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000616721 |
| Start | 39885991:39885991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746925769 |
| CDS Mutation | c.8188C>T |
| AA Mutation | p.Pro2730Ser(p.P2730S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39873425:39873425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140593694 |
| CDS Mutation | c.10974C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39915251:39915251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2763C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39891983:39891983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6660C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39894490:39894490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5271C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39872208:39872208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11619C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39872532:39872532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763153692 |
| CDS Mutation | c.11295C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39878030:39878030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750357330 |
| CDS Mutation | c.9075T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39893475:39893475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5892G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39891758:39891758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773651497 |
| CDS Mutation | c.6885C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39891707:39891707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6936C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39927186:39927186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148301068 |
| CDS Mutation | c.1176G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39928110:39928110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368985940 |
| CDS Mutation | c.252C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39873755:39873755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10644T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39891740:39891740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6903C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39891956:39891956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6687C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39889812:39889812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7260C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39892154:39892154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6489G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 67 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39875668:39875668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs530920778 |
| CDS Mutation | c.10323C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 68 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39927966:39927966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.396G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 69 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39927144:39927144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747430249 |
| CDS Mutation | c.1218G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 70 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39891686:39891686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6957C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 71 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39877694:39877694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9411C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 72 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39875545:39875545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778297878 |
| CDS Mutation | c.10446C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 73 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39892031:39892031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772696382 |
| CDS Mutation | c.6612G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 74 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39894145:39894145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5616C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 75 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000616721 |
| Start | 39915214:39915214(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2800delG |
| AA Mutation | p.Val934CysfsTer44(p.V934Cfs*44) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 76 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000616721 |
| Start | 39895952:39895952(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5119delG |
| AA Mutation | p.Val1707SerfsTer6(p.V1707Sfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 77 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000616721 |
| Start | 39879801:39879801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8622C>A |
| AA Mutation | p.Cys2874Ter(p.C2874*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 78 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000616721 |
| Start | 39927914:39927915(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs765680504 |
| CDS Mutation | c.447dupC |
| AA Mutation | p.Gly150ArgfsTer68(p.G150Rfs*68) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 79 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000616721 |
| Start | 39872534:39872536(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.11291_11293delATG |
| AA Mutation | p.Asp3764del(p.D3764del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |