Primary Site >> Stomach Cancer
Gene >> WNT10B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301061 |
| Start | 48967950:48967950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372388862 |
| CDS Mutation | c.707G>A |
| AA Mutation | p.Arg236His(p.R236H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301061 |
| Start | 48968040:48968040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.617G>C |
| AA Mutation | p.Gly206Ala(p.G206A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301061 |
| Start | 48966165:48966165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745726077 |
| CDS Mutation | c.1100G>A |
| AA Mutation | p.Arg367His(p.R367H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301061 |
| Start | 48968120:48968120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.537C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301061 |
| Start | 48970494:48970494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373412829 |
| CDS Mutation | c.36G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000301061 |
| Start | 48968099:48968099(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.558delC |
| AA Mutation | p.Ser187AlafsTer53(p.S187Afs*53) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |