Primary Site >> Stomach Cancer
Gene >> TRAF6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348124 |
| Start | 36498636:36498636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.301G>A |
| AA Mutation | p.Ala101Thr(p.A101T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348124 |
| Start | 36494989:36494989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.665T>C |
| AA Mutation | p.Leu222Pro(p.L222P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348124 |
| Start | 36490464:36490464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.943G>A |
| AA Mutation | p.Glu315Lys(p.E315K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348124 |
| Start | 36490565:36490565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.842G>A |
| AA Mutation | p.Ser281Asn(p.S281N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348124 |
| Start | 36489855:36489855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1552A>G |
| AA Mutation | p.Thr518Ala(p.T518A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348124 |
| Start | 36490214:36490214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1193C>T |
| AA Mutation | p.Pro398Leu(p.P398L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348124 |
| Start | 36489850:36489850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1557T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348124 |
| Start | 36490252:36490252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777821743 |
| CDS Mutation | c.1155C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |