Primary Site >> Stomach Cancer
Gene >> TRAF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373887 |
| Start | 120923785:120923785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368092786 |
| CDS Mutation | c.148G>A |
| AA Mutation | p.Glu50Lys(p.E50K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373887 |
| Start | 120911383:120911383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547890013 |
| CDS Mutation | c.836G>A |
| AA Mutation | p.Arg279Gln(p.R279Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373887 |
| Start | 120913458:120913458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.575G>T |
| AA Mutation | p.Gly192Val(p.G192V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373887 |
| Start | 120913350:120913350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373510970 |
| CDS Mutation | c.683G>A |
| AA Mutation | p.Arg228His(p.R228H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373887 |
| Start | 120926044:120926044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779984358 |
| CDS Mutation | c.32C>T |
| AA Mutation | p.Pro11Leu(p.P11L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373887 |
| Start | 120923725:120923725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.208C>T |
| AA Mutation | p.Arg70Cys(p.R70C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373887 |
| Start | 120923786:120923786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.147C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373887 |
| Start | 120909293:120909293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746395490 |
| CDS Mutation | c.969G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |