Primary Site >> Stomach Cancer
Gene >> VWCE
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335613 |
| Start | 61264967:61264967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2128T>C |
| AA Mutation | p.Cys710Arg(p.C710R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335613 |
| Start | 61286329:61286329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.526C>T |
| AA Mutation | p.Arg176Cys(p.R176C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335613 |
| Start | 61274516:61274516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1564A>G |
| AA Mutation | p.Thr522Ala(p.T522A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335613 |
| Start | 61281116:61281116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764490792 |
| CDS Mutation | c.907C>T |
| AA Mutation | p.Pro303Ser(p.P303S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335613 |
| Start | 61281145:61281145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.878G>T |
| AA Mutation | p.Arg293Leu(p.R293L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335613 |
| Start | 61273271:61273271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1627T>C |
| AA Mutation | p.Cys543Arg(p.C543R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335613 |
| Start | 61291340:61291340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.219C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335613 |
| Start | 61280796:61280796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1227C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000335613 |
| Start | 61258692:61258692(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs775714858 |
| CDS Mutation | c.2851delG |
| AA Mutation | p.Glu951LysfsTer33(p.E951Kfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |