Primary Site >> Stomach Cancer
Gene >> DISP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284476 |
| Start | 223003663:223003663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766010478 |
| CDS Mutation | c.2266C>T |
| AA Mutation | p.Arg756Trp(p.R756W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284476 |
| Start | 223003684:223003684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759714329 |
| CDS Mutation | c.2287C>T |
| AA Mutation | p.Arg763Cys(p.R763C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284476 |
| Start | 223004341:223004341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762072719 |
| CDS Mutation | c.2944G>A |
| AA Mutation | p.Asp982Asn(p.D982N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284476 |
| Start | 223003222:223003222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1825T>C |
| AA Mutation | p.Phe609Leu(p.F609L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284476 |
| Start | 223004404:223004404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3007A>C |
| AA Mutation | p.Thr1003Pro(p.T1003P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284476 |
| Start | 223002472:223002472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747659889 |
| CDS Mutation | c.1075G>A |
| AA Mutation | p.Ala359Thr(p.A359T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284476 |
| Start | 223003037:223003037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765609888 |
| CDS Mutation | c.1640G>A |
| AA Mutation | p.Arg547His(p.R547H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284476 |
| Start | 223003378:223003378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369217520 |
| CDS Mutation | c.1981C>T |
| AA Mutation | p.Arg661Trp(p.R661W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284476 |
| Start | 223003883:223003883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2486A>G |
| AA Mutation | p.His829Arg(p.H829R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284476 |
| Start | 223005910:223005910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4513G>A |
| AA Mutation | p.Val1505Met(p.V1505M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284476 |
| Start | 223002835:223002835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1438G>A |
| AA Mutation | p.Gly480Ser(p.G480S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284476 |
| Start | 223003480:223003480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2083C>G |
| AA Mutation | p.Leu695Val(p.L695V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284476 |
| Start | 223003247:223003247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749431977 |
| CDS Mutation | c.1850C>T |
| AA Mutation | p.Ala617Val(p.A617V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284476 |
| Start | 223005168:223005168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3771A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284476 |
| Start | 223003344:223003344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1947C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284476 |
| Start | 223005330:223005330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747624147 |
| CDS Mutation | c.3933C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284476 |
| Start | 223003851:223003851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764747224 |
| CDS Mutation | c.2454C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284476 |
| Start | 223005231:223005231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3834A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284476 |
| Start | 223004085:223004085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2688G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284476 |
| Start | 223004340:223004340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201988727 |
| CDS Mutation | c.2943C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284476 |
| Start | 223003773:223003773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753722465 |
| CDS Mutation | c.2376C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284476 |
| Start | 223004532:223004532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3135C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284476 |
| Start | 222990661:222990661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.576C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284476 |
| Start | 223005387:223005387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370266646 |
| CDS Mutation | c.3990G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284476 |
| Start | 222990664:222990664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.579G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284476 |
| Start | 223003968:223003968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2571A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284476 |
| Start | 223004631:223004631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771089164 |
| CDS Mutation | c.3234C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000284476 |
| Start | 223004836:223004836(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3444delA |
| AA Mutation | p.Lys1148AsnfsTer26(p.K1148Nfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000284476 |
| Start | 222991643:222991643(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.790delA |
| AA Mutation | p.Ser264AlafsTer62(p.S264Afs*62) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000284476 |
| Start | 222991580:222991580(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.728delA |
| AA Mutation | p.Asn243IlefsTer8(p.N243Ifs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000284476 |
| Start | 223003288:223003288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747887655 |
| CDS Mutation | c.1891C>T |
| AA Mutation | p.Arg631Ter(p.R631*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |