Primary Site >> Stomach Cancer
Gene >> TRPC3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379645 |
| Start | 121879848:121879848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2654C>A |
| AA Mutation | p.Ser885Tyr(p.S885Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379645 |
| Start | 121932644:121932644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.614G>A |
| AA Mutation | p.Arg205His(p.R205H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379645 |
| Start | 121932650:121932650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.608G>T |
| AA Mutation | p.Ser203Ile(p.S203I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379645 |
| Start | 121932471:121932471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.787C>T |
| AA Mutation | p.His263Tyr(p.H263Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379645 |
| Start | 121932687:121932687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.571G>A |
| AA Mutation | p.Val191Ile(p.V191I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379645 |
| Start | 121899685:121899685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2474T>C |
| AA Mutation | p.Phe825Ser(p.F825S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379645 |
| Start | 121925173:121925173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1021G>A |
| AA Mutation | p.Asp341Asn(p.D341N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379645 |
| Start | 121932696:121932696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.562G>A |
| AA Mutation | p.Val188Met(p.V188M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379645 |
| Start | 121932740:121932740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.518C>T |
| AA Mutation | p.Ala173Val(p.A173V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379645 |
| Start | 121932840:121932840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770588520 |
| CDS Mutation | c.418G>A |
| AA Mutation | p.Val140Ile(p.V140I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379645 |
| Start | 121932493:121932493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.765G>T |
| AA Mutation | p.Lys255Asn(p.K255N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379645 |
| Start | 121932476:121932476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.782G>A |
| AA Mutation | p.Arg261Gln(p.R261Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379645 |
| Start | 121911979:121911979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1456A>C |
| AA Mutation | p.Thr486Pro(p.T486P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379645 |
| Start | 121932983:121932983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.275G>A |
| AA Mutation | p.Arg92His(p.R92H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379645 |
| Start | 121932604:121932604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766293867 |
| CDS Mutation | c.654C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379645 |
| Start | 121932739:121932739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201407818 |
| CDS Mutation | c.519G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379645 |
| Start | 121911887:121911887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1548C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379645 |
| Start | 121910242:121910242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201887788 |
| CDS Mutation | c.1704G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |