Primary Site >> Stomach Cancer
Gene >> TNFRSF1B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376259 |
| Start | 12191882:12191882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765864632 |
| CDS Mutation | c.416C>T |
| AA Mutation | p.Pro139Leu(p.P139L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376259 |
| Start | 12207016:12207016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1382G>A |
| AA Mutation | p.Ser461Asn(p.S461N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376259 |
| Start | 12188890:12188890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139221787 |
| CDS Mutation | c.173C>T |
| AA Mutation | p.Ser58Leu(p.S58L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376259 |
| Start | 12191895:12191895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.429C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376259 |
| Start | 12202008:12202008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375369071 |
| CDS Mutation | c.942C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376259 |
| Start | 12202092:12202092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776068574 |
| CDS Mutation | c.1026G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000376259 |
| Start | 12206739:12206739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1106-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |