Primary Site >> Stomach Cancer
Gene >> STT3A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392708 |
| Start | 125602349:125602349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.196T>C |
| AA Mutation | p.Tyr66His(p.Y66H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392708 |
| Start | 125606421:125606421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.736C>A |
| AA Mutation | p.Leu246Met(p.L246M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392708 |
| Start | 125614091:125614091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376733157 |
| CDS Mutation | c.1559C>T |
| AA Mutation | p.Ala520Val(p.A520V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392708 |
| Start | 125602347:125602347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.194T>C |
| AA Mutation | p.Phe65Ser(p.F65S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392708 |
| Start | 125618387:125618387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1789C>A |
| AA Mutation | p.Leu597Ile(p.L597I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392708 |
| Start | 125608127:125608127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.799C>T |
| AA Mutation | p.His267Tyr(p.H267Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392708 |
| Start | 125605658:125605658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.538T>C |
| AA Mutation | p.Tyr180His(p.Y180H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392708 |
| Start | 125614334:125614334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1682C>A |
| AA Mutation | p.Ser561Tyr(p.S561Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392708 |
| Start | 125608204:125608204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.876A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392708 |
| Start | 125606426:125606426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1051714 |
| CDS Mutation | c.741C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |