Primary Site >> Stomach Cancer
Gene >> ANO9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332826 |
| Start | 418746:418746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758562981 |
| CDS Mutation | c.2104C>T |
| AA Mutation | p.Arg702Cys(p.R702C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332826 |
| Start | 420496:420496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1753C>T |
| AA Mutation | p.Arg585Trp(p.R585W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332826 |
| Start | 419621:419621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759531921 |
| CDS Mutation | c.1895G>A |
| AA Mutation | p.Arg632His(p.R632H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332826 |
| Start | 428612:428612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199703326 |
| CDS Mutation | c.1048G>A |
| AA Mutation | p.Val350Ile(p.V350I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332826 |
| Start | 428112:428112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1310T>C |
| AA Mutation | p.Ile437Thr(p.I437T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332826 |
| Start | 429589:429589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.896A>G |
| AA Mutation | p.Tyr299Cys(p.Y299C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332826 |
| Start | 428597:428597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764201726 |
| CDS Mutation | c.1063C>T |
| AA Mutation | p.Arg355Cys(p.R355C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332826 |
| Start | 420541:420541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1708C>A |
| AA Mutation | p.Leu570Ile(p.L570I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332826 |
| Start | 428382:428382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139493381 |
| CDS Mutation | c.1198G>A |
| AA Mutation | p.Val400Met(p.V400M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332826 |
| Start | 431736:431736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372316223 |
| CDS Mutation | c.497G>A |
| AA Mutation | p.Arg166Gln(p.R166Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332826 |
| Start | 431745:431745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181550038 |
| CDS Mutation | c.488C>T |
| AA Mutation | p.Thr163Met(p.T163M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332826 |
| Start | 432030:432030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751240755 |
| CDS Mutation | c.375C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332826 |
| Start | 428583:428583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115389769 |
| CDS Mutation | c.1077C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332826 |
| Start | 421037:421037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752391643 |
| CDS Mutation | c.1398C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332826 |
| Start | 418560:418560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375331821 |
| CDS Mutation | c.2160C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332826 |
| Start | 418410:418410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2310C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000332826 |
| Start | 418445:418445(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs761382318 |
| CDS Mutation | c.2275delG |
| AA Mutation | p.Ala759GlnfsTer36(p.A759Qfs*36) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |