Primary Site >> Stomach Cancer
Gene >> MAP3K8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263056 |
| Start | 30459268:30459268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1040C>T |
| AA Mutation | p.Ala347Val(p.A347V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263056 |
| Start | 30447821:30447821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201540136 |
| CDS Mutation | c.376G>A |
| AA Mutation | p.Asp126Asn(p.D126N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263056 |
| Start | 30450338:30450338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777369971 |
| CDS Mutation | c.585C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263056 |
| Start | 30460713:30460713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150841663 |
| CDS Mutation | c.1281G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263056 |
| Start | 30447886:30447886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200843234 |
| CDS Mutation | c.441C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263056 |
| Start | 30450329:30450329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755618467 |
| CDS Mutation | c.576G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263056 |
| Start | 30460728:30460728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369517029 |
| CDS Mutation | c.1296C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263056 |
| Start | 30459326:30459326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1098A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263056 |
| Start | 30459398:30459398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141896473 |
| CDS Mutation | c.1170G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |