Primary Site >> Stomach Cancer
Gene >> FASLG
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367721 |
| Start | 172665973:172665973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.803A>T |
| AA Mutation | p.Asn268Ile(p.N268I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367721 |
| Start | 172665639:172665639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.469T>C |
| AA Mutation | p.Ser157Pro(p.S157P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367721 |
| Start | 172665772:172665772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.602C>A |
| AA Mutation | p.Ser201Tyr(p.S201Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367721 |
| Start | 172665759:172665759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776079129 |
| CDS Mutation | c.589T>C |
| AA Mutation | p.Phe197Leu(p.F197L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367721 |
| Start | 172659384:172659384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755282797 |
| CDS Mutation | c.183A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367721 |
| Start | 172666010:172666010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749748178 |
| CDS Mutation | c.840G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000367721 |
| Start | 172659270:172659270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.69G>A |
| AA Mutation | p.Trp23Ter(p.W23*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |