Primary Site >> Stomach Cancer
Gene >> TNFAIP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226225 |
| Start | 28344455:28344455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.806C>T |
| AA Mutation | p.Ala269Val(p.A269V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226225 |
| Start | 28342371:28342371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.643G>A |
| AA Mutation | p.Gly215Ser(p.G215S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226225 |
| Start | 28344559:28344559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.910G>A |
| AA Mutation | p.Asp304Asn(p.D304N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226225 |
| Start | 28344421:28344421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.772A>T |
| AA Mutation | p.Thr258Ser(p.T258S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000226225 |
| Start | 28342310:28342310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs77434228 |
| CDS Mutation | c.582C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000226225 |
| Start | 28339668:28339668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781935759 |
| CDS Mutation | c.147C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |