Primary Site >> Stomach Cancer
Gene >> VPS41
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310301 |
| Start | 38763465:38763465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1412G>A |
| AA Mutation | p.Ser471Asn(p.S471N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310301 |
| Start | 38869211:38869211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.103C>A |
| AA Mutation | p.Leu35Ile(p.L35I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310301 |
| Start | 38752271:38752271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761915762 |
| CDS Mutation | c.1831C>T |
| AA Mutation | p.Arg611Cys(p.R611C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000310301 |
| Start | 38756980:38756980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566849862 |
| CDS Mutation | c.1553A>G |
| AA Mutation | p.Tyr518Cys(p.Y518C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310301 |
| Start | 38758417:38758417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1487C>T |
| AA Mutation | p.Ala496Val(p.A496V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310301 |
| Start | 38743411:38743411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2113G>A |
| AA Mutation | p.Asp705Asn(p.D705N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310301 |
| Start | 38752232:38752232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1870G>A |
| AA Mutation | p.Asp624Asn(p.D624N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310301 |
| Start | 38752262:38752262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1840G>A |
| AA Mutation | p.Glu614Lys(p.E614K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310301 |
| Start | 38752235:38752235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1867T>A |
| AA Mutation | p.Tyr623Asn(p.Y623N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310301 |
| Start | 38758410:38758410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1494G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310301 |
| Start | 38743472:38743472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373593442 |
| CDS Mutation | c.2052C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310301 |
| Start | 38726294:38726294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2517T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000310301 |
| Start | 38830300:38830300(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.275delT |
| AA Mutation | p.Leu92TrpfsTer46(p.L92Wfs*46) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000310301 |
| Start | 38771220:38771220(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs757692785 |
| CDS Mutation | c.1163delA |
| AA Mutation | p.Asn388IlefsTer15(p.N388Ifs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000310301 |
| Start | 38772575:38772575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779846421 |
| CDS Mutation | c.1075G>T |
| AA Mutation | p.Glu359Ter(p.E359*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |