Primary Site >> Stomach Cancer
Gene >> STAT3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264657 |
| Start | 42322402:42322402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747639500 |
| CDS Mutation | c.1981G>T |
| AA Mutation | p.Asp661Tyr(p.D661Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264657 |
| Start | 42337536:42337536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.696G>T |
| AA Mutation | p.Gln232His(p.Q232H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264657 |
| Start | 42324795:42324795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1516G>A |
| AA Mutation | p.Glu506Lys(p.E506K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264657 |
| Start | 42322422:42322422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1961T>C |
| AA Mutation | p.Ile654Thr(p.I654T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264657 |
| Start | 42329582:42329582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1205G>A |
| AA Mutation | p.Gly402Asp(p.G402D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264657 |
| Start | 42337510:42337510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.722C>A |
| AA Mutation | p.Ala241Asp(p.A241D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264657 |
| Start | 42315769:42315769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147202525 |
| CDS Mutation | c.2289G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264657 |
| Start | 42324978:42324978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1449G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264657 |
| Start | 42322463:42322463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751536580 |
| CDS Mutation | c.1920C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |