Primary Site >> Stomach Cancer
Gene >> STON1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000404752 |
| Start | 48582273:48582273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1640T>C |
| AA Mutation | p.Val547Ala(p.V547A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000404752 |
| Start | 48582478:48582478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1845T>G |
| AA Mutation | p.Ile615Met(p.I615M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000404752 |
| Start | 48581649:48581649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1016G>A |
| AA Mutation | p.Ser339Asn(p.S339N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000404752 |
| Start | 48582239:48582239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1606G>A |
| AA Mutation | p.Val536Ile(p.V536I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000404752 |
| Start | 48581636:48581636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752820573 |
| CDS Mutation | c.1003G>A |
| AA Mutation | p.Val335Ile(p.V335I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000404752 |
| Start | 48581792:48581792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1159C>A |
| AA Mutation | p.Leu387Ile(p.L387I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000404752 |
| Start | 48581369:48581369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.736A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000404752 |
| Start | 48581665:48581665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1032C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000404752 |
| Start | 48581617:48581617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs572264454 |
| CDS Mutation | c.984T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000404752 |
| Start | 48582292:48582292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370458736 |
| CDS Mutation | c.1659G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |