Primary Site >> Stomach Cancer
Gene >> WNT7B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339464 |
| Start | 45949976:45949976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768081658 |
| CDS Mutation | c.242G>A |
| AA Mutation | p.Arg81His(p.R81H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339464 |
| Start | 45923166:45923166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769997103 |
| CDS Mutation | c.740G>A |
| AA Mutation | p.Arg247Gln(p.R247Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339464 |
| Start | 45931268:45931268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202233642 |
| CDS Mutation | c.400G>A |
| AA Mutation | p.Asp134Asn(p.D134N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339464 |
| Start | 45923004:45923004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61735041 |
| CDS Mutation | c.902C>T |
| AA Mutation | p.Ala301Val(p.A301V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339464 |
| Start | 45923011:45923011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.895C>T |
| AA Mutation | p.Pro299Ser(p.P299S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339464 |
| Start | 45923084:45923084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373897406 |
| CDS Mutation | c.822G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |