Primary Site >> Stomach Cancer
Gene >> VWF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6013543:6013543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5558G>A |
| AA Mutation | p.Arg1853Gln(p.R1853Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6011697:6011697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770879215 |
| CDS Mutation | c.5762G>A |
| AA Mutation | p.Arg1921Gln(p.R1921Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6023718:6023718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755385279 |
| CDS Mutation | c.3292G>A |
| AA Mutation | p.Ala1098Thr(p.A1098T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6072361:6072361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1079G>A |
| AA Mutation | p.Gly360Asp(p.G360D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6023670:6023670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3340C>T |
| AA Mutation | p.His1114Tyr(p.H1114Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6019142:6019142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555366738 |
| CDS Mutation | c.4276C>T |
| AA Mutation | p.Arg1426Cys(p.R1426C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 5996094:5996094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5971G>A |
| AA Mutation | p.Gly1991Ser(p.G1991S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6019638:6019638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3780G>T |
| AA Mutation | p.Glu1260Asp(p.E1260D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 5994186:5994186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767280593 |
| CDS Mutation | c.6274G>A |
| AA Mutation | p.Gly2092Arg(p.G2092R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 5949829:5949829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8210G>T |
| AA Mutation | p.Gly2737Val(p.G2737V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6018619:6018619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376943868 |
| CDS Mutation | c.4799C>T |
| AA Mutation | p.Ala1600Val(p.A1600V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 5994005:5994005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6455A>T |
| AA Mutation | p.Lys2152Met(p.K2152M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6016633:6016633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5194G>A |
| AA Mutation | p.Val1732Met(p.V1732M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6019213:6019213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4205A>G |
| AA Mutation | p.Gln1402Arg(p.Q1402R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 5996165:5996165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5900A>C |
| AA Mutation | p.Lys1967Thr(p.K1967T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6019138:6019138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4280T>G |
| AA Mutation | p.Leu1427Arg(p.L1427R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6052720:6052720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2009G>A |
| AA Mutation | p.Arg670His(p.R670H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 5991947:5991947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6670G>A |
| AA Mutation | p.Val2224Met(p.V2224M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6019393:6019393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs527483960 |
| CDS Mutation | c.4025G>A |
| AA Mutation | p.Arg1342His(p.R1342H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 5949086:5949086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8371G>T |
| AA Mutation | p.Gly2791Cys(p.G2791C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6019378:6019378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4040T>C |
| AA Mutation | p.Val1347Ala(p.V1347A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6110933:6110933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140044866 |
| CDS Mutation | c.256G>A |
| AA Mutation | p.Val86Met(p.V86M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 5971628:5971628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368286307 |
| CDS Mutation | c.7519C>T |
| AA Mutation | p.Arg2507Trp(p.R2507W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6019549:6019549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3869A>T |
| AA Mutation | p.Glu1290Val(p.E1290V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6044388:6044388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61748472 |
| CDS Mutation | c.2345G>A |
| AA Mutation | p.Arg782Gln(p.R782Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 5981922:5981922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150201871 |
| CDS Mutation | c.7151G>A |
| AA Mutation | p.Arg2384Gln(p.R2384Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6121243:6121243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.151T>C |
| AA Mutation | p.Tyr51His(p.Y51H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 5969255:5969255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7685A>C |
| AA Mutation | p.Gln2562Pro(p.Q2562P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 5971612:5971612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7535C>A |
| AA Mutation | p.Ser2512Tyr(p.S2512Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6121267:6121267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772466729 |
| CDS Mutation | c.127G>A |
| AA Mutation | p.Val43Ile(p.V43I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261405 |
| Start | 6052592:6052592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2137G>A |
| AA Mutation | p.Gly713Ser(p.G713S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261405 |
| Start | 6057868:6057868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1710C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261405 |
| Start | 6018918:6018918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs560049911 |
| CDS Mutation | c.4500G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261405 |
| Start | 6095490:6095490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.627A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261405 |
| Start | 6029357:6029357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2952G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261405 |
| Start | 5949801:5949801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8238T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261405 |
| Start | 5994094:5994094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141097321 |
| CDS Mutation | c.6366G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261405 |
| Start | 5985609:5985609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745659470 |
| CDS Mutation | c.6855C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261405 |
| Start | 6013569:6013569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754986617 |
| CDS Mutation | c.5532C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261405 |
| Start | 5993905:5993905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6555G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261405 |
| Start | 6019647:6019647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3771G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261405 |
| Start | 5991969:5991969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6648T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261405 |
| Start | 6021965:6021965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3609C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261405 |
| Start | 6018618:6018618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201264909 |
| CDS Mutation | c.4800G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261405 |
| Start | 6019004:6019004(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.4414delG |
| AA Mutation | p.Asp1472ThrfsTer53(p.D1472Tfs*53) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261405 |
| Start | 6044298:6044298(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs62643632 |
| CDS Mutation | c.2435delC |
| AA Mutation | p.Pro812ArgfsTer31(p.P812Rfs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261405 |
| Start | 6044423:6044423(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs776747320 |
| CDS Mutation | c.2310delC |
| AA Mutation | p.Met771TrpfsTer30(p.M771Wfs*30) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |