Primary Site >> Stomach Cancer
Gene >> WNT16
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222462 |
| Start | 121339182:121339182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554766007 |
| CDS Mutation | c.935G>A |
| AA Mutation | p.Arg312His(p.R312H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222462 |
| Start | 121331893:121331893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780579430 |
| CDS Mutation | c.562G>A |
| AA Mutation | p.Gly188Arg(p.G188R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222462 |
| Start | 121339251:121339251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1004G>T |
| AA Mutation | p.Arg335Met(p.R335M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222462 |
| Start | 121339238:121339238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.991A>G |
| AA Mutation | p.Thr331Ala(p.T331A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222462 |
| Start | 121339328:121339328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1081G>A |
| AA Mutation | p.Val361Ile(p.V361I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222462 |
| Start | 121338886:121338886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201359695 |
| CDS Mutation | c.639C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222462 |
| Start | 121331825:121331825(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs773332445 |
| CDS Mutation | c.500delG |
| AA Mutation | p.Gly167AlafsTer17(p.G167Afs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |