Primary Site >> Stomach Cancer
Gene >> STAT6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300134 |
| Start | 57105549:57105549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768675729 |
| CDS Mutation | c.731C>T |
| AA Mutation | p.Ala244Val(p.A244V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300134 |
| Start | 57099820:57099820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1691G>T |
| AA Mutation | p.Ser564Ile(p.S564I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300134 |
| Start | 57104794:57104794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1021A>C |
| AA Mutation | p.Ile341Leu(p.I341L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300134 |
| Start | 57107255:57107255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.315A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300134 |
| Start | 57107695:57107695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.165C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300134 |
| Start | 57105512:57105512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559027154 |
| CDS Mutation | c.768G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |