Primary Site >> Stomach Cancer
Gene >> PTPRT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42085771:42085771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3929A>C |
| AA Mutation | p.Glu1310Ala(p.E1310A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42081963:42081963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4191G>A |
| AA Mutation | p.Met1397Ile(p.M1397I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42791416:42791416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.265C>A |
| AA Mutation | p.His89Asn(p.H89N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42098437:42098437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3830A>C |
| AA Mutation | p.Glu1277Ala(p.E1277A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42102211:42102211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3627G>T |
| AA Mutation | p.Met1209Ile(p.M1209I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42472470:42472470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1246C>T |
| AA Mutation | p.Arg416Cys(p.R416C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42106830:42106830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761910971 |
| CDS Mutation | c.3346G>A |
| AA Mutation | p.Val1116Met(p.V1116M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42885902:42885902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.119A>G |
| AA Mutation | p.Asn40Ser(p.N40S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42161530:42161530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373191879 |
| CDS Mutation | c.2504G>A |
| AA Mutation | p.Arg835His(p.R835H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42791385:42791385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.296A>G |
| AA Mutation | p.Asp99Gly(p.D99G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42161444:42161444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2590C>A |
| AA Mutation | p.Gln864Lys(p.Q864K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42678156:42678156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.863C>A |
| AA Mutation | p.Pro288His(p.P288H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42315975:42315975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1887G>T |
| AA Mutation | p.Lys629Asn(p.K629N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42115252:42115252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3046A>G |
| AA Mutation | p.Ile1016Val(p.I1016V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42115273:42115273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375441200 |
| CDS Mutation | c.3025G>A |
| AA Mutation | p.Gly1009Arg(p.G1009R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42756537:42756537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201332786 |
| CDS Mutation | c.784G>A |
| AA Mutation | p.Val262Ile(p.V262I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42084697:42084697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4121C>T |
| AA Mutation | p.Thr1374Ile(p.T1374I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42282504:42282504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776134993 |
| CDS Mutation | c.2161C>T |
| AA Mutation | p.Arg721Cys(p.R721C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42677943:42677943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571224137 |
| CDS Mutation | c.1076G>A |
| AA Mutation | p.Arg359Gln(p.R359Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42161528:42161528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745346735 |
| CDS Mutation | c.2506G>A |
| AA Mutation | p.Gly836Arg(p.G836R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42248814:42248814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2185A>C |
| AA Mutation | p.Thr729Pro(p.T729P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42084791:42084791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4027T>A |
| AA Mutation | p.Tyr1343Asn(p.Y1343N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42236233:42236233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2338T>C |
| AA Mutation | p.Tyr780His(p.Y780H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42472556:42472556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1160T>G |
| AA Mutation | p.Val387Gly(p.V387G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42110384:42110384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3203A>C |
| AA Mutation | p.Gln1068Pro(p.Q1068P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42118437:42118437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2948T>C |
| AA Mutation | p.Ile983Thr(p.I983T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42472514:42472514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200302453 |
| CDS Mutation | c.1202G>A |
| AA Mutation | p.Arg401Gln(p.R401Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42791311:42791311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.370G>A |
| AA Mutation | p.Val124Met(p.V124M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42315976:42315976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1886A>C |
| AA Mutation | p.Lys629Thr(p.K629T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42248778:42248778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2221G>A |
| AA Mutation | p.Val741Met(p.V741M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42161389:42161389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2645A>C |
| AA Mutation | p.Lys882Thr(p.K882T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42677974:42677974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1045C>T |
| AA Mutation | p.His349Tyr(p.H349Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42104587:42104587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3522A>C |
| AA Mutation | p.Gln1174His(p.Q1174H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42102275:42102275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753788938 |
| CDS Mutation | c.3563G>A |
| AA Mutation | p.Arg1188His(p.R1188H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42106827:42106827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776642212 |
| CDS Mutation | c.3349C>T |
| AA Mutation | p.Arg1117Cys(p.R1117C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42102210:42102210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3628G>T |
| AA Mutation | p.Asp1210Tyr(p.D1210Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42678147:42678147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.872C>A |
| AA Mutation | p.Pro291His(p.P291H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42352137:42352137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1709C>A |
| AA Mutation | p.Thr570Lys(p.T570K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42118463:42118463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2922G>A |
| AA Mutation | p.Met974Ile(p.M974I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42098437:42098437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3830A>T |
| AA Mutation | p.Glu1277Val(p.E1277V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42118449:42118449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2936A>G |
| AA Mutation | p.Asn979Ser(p.N979S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42315964:42315964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1898T>G |
| AA Mutation | p.Leu633Arg(p.L633R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42352210:42352210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752620539 |
| CDS Mutation | c.1636C>T |
| AA Mutation | p.Arg546Trp(p.R546W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373187 |
| Start | 42352176:42352176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1670A>G |
| AA Mutation | p.Tyr557Cys(p.Y557C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000373187 |
| Start | 42085851:42085851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3849C>A |
| AA Mutation | p.Phe1283Leu(p.F1283L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42199253:42199253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751682847 |
| CDS Mutation | c.2478C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42084780:42084780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751405410 |
| CDS Mutation | c.4038G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42102208:42102208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs35010609 |
| CDS Mutation | c.3630C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42677971:42677971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1048C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42780234:42780234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368788783 |
| CDS Mutation | c.552C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42161517:42161517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2517C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42084714:42084714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370589712 |
| CDS Mutation | c.4104C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42677891:42677891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1128C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42791318:42791318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372820451 |
| CDS Mutation | c.363C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42472315:42472315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375501287 |
| CDS Mutation | c.1401C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42085791:42085791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs34623060 |
| CDS Mutation | c.3909C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42780258:42780258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.528C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42098535:42098535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754824702 |
| CDS Mutation | c.3732C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42106831:42106831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189118400 |
| CDS Mutation | c.3345C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373187 |
| Start | 42248803:42248803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2196T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373187 |
| Start | 42677913:42677913(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1106delG |
| AA Mutation | p.Gly369ValfsTer28(p.G369Vfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373187 |
| Start | 42110363:42110363(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3224delC |
| AA Mutation | p.Pro1075ArgfsTer6(p.P1075Rfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373187 |
| Start | 42110369:42110369(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3218delA |
| AA Mutation | p.Asn1073ThrfsTer8(p.N1073Tfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000373187 |
| Start | 42161373:42161373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2661C>A |
| AA Mutation | p.Tyr887Ter(p.Y887*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000373187 |
| Start | 42472335:42472335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1381C>T |
| AA Mutation | p.Arg461Ter(p.R461*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000373187 |
| Start | 42115303:42115303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763964405 |
| CDS Mutation | c.2995C>T |
| AA Mutation | p.Arg999Ter(p.R999*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |