Primary Site >> Stomach Cancer
Gene >> ANO1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355303 |
| Start | 70161263:70161263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1681C>T |
| AA Mutation | p.Arg561Trp(p.R561W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355303 |
| Start | 70182547:70182547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2449T>C |
| AA Mutation | p.Tyr817His(p.Y817H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355303 |
| Start | 70149749:70149749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1298G>A |
| AA Mutation | p.Arg433Gln(p.R433Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355303 |
| Start | 70161264:70161264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763424037 |
| CDS Mutation | c.1682G>A |
| AA Mutation | p.Arg561Gln(p.R561Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355303 |
| Start | 70170962:70170962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2273T>G |
| AA Mutation | p.Ile758Ser(p.I758S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355303 |
| Start | 70187749:70187749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2706G>A |
| AA Mutation | p.Met902Ile(p.M902I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355303 |
| Start | 70087960:70087960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373880950 |
| CDS Mutation | c.317C>T |
| AA Mutation | p.Ala106Val(p.A106V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355303 |
| Start | 70187996:70187996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201685852 |
| CDS Mutation | c.2953G>A |
| AA Mutation | p.Val985Ile(p.V985I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355303 |
| Start | 70153077:70153077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369762692 |
| CDS Mutation | c.1374C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355303 |
| Start | 70131961:70131961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745644830 |
| CDS Mutation | c.1140G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |