Primary Site >> Stomach Cancer
Gene >> MAP3K1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399503 |
| Start | 56881757:56881757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368201444 |
| CDS Mutation | c.2557C>T |
| AA Mutation | p.Arg853Cys(p.R853C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399503 |
| Start | 56885938:56885938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3989C>T |
| AA Mutation | p.Ser1330Leu(p.S1330L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399503 |
| Start | 56881761:56881761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2561G>A |
| AA Mutation | p.Arg854His(p.R854H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399503 |
| Start | 56882396:56882396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3196A>G |
| AA Mutation | p.Thr1066Ala(p.T1066A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399503 |
| Start | 56872886:56872886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1567G>A |
| AA Mutation | p.Val523Ile(p.V523I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399503 |
| Start | 56883568:56883568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774493506 |
| CDS Mutation | c.3708G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |