Primary Site >> Stomach Cancer
Gene >> AAAS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000209873 |
| Start | 53314304:53314304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.683C>G |
| AA Mutation | p.Ser228Cys(p.S228C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000209873 |
| Start | 53307581:53307581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1549C>A |
| AA Mutation | p.Leu517Ile(p.L517I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000209873 |
| Start | 53307858:53307858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1403C>T |
| AA Mutation | p.Ala468Val(p.A468V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000209873 |
| Start | 53307689:53307689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1441C>T |
| AA Mutation | p.His481Tyr(p.H481Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000209873 |
| Start | 53308347:53308347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766356863 |
| CDS Mutation | c.1184T>C |
| AA Mutation | p.Leu395Pro(p.L395P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000209873 |
| Start | 53309196:53309196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.896G>A |
| AA Mutation | p.Gly299Asp(p.G299D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000209873 |
| Start | 53307607:53307607(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1523delG |
| AA Mutation | p.Gly508ValfsTer43(p.G508Vfs*43) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000209873 |
| Start | 53307895:53307895(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs767701527 |
| CDS Mutation | c.1366delC |
| AA Mutation | p.Gln456SerfsTer95(p.Q456Sfs*95) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |