Primary Site >> Stomach Cancer
Gene >> WNT7A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285018 |
| Start | 13854615:13854615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772935313 |
| CDS Mutation | c.487G>A |
| AA Mutation | p.Ala163Thr(p.A163T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285018 |
| Start | 13854777:13854777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs104893832 |
| CDS Mutation | c.325G>A |
| AA Mutation | p.Ala109Thr(p.A109T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285018 |
| Start | 13818970:13818970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1024C>T |
| AA Mutation | p.Arg342Cys(p.R342C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285018 |
| Start | 13854573:13854573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746475689 |
| CDS Mutation | c.529C>T |
| AA Mutation | p.Arg177Trp(p.R177W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285018 |
| Start | 13854749:13854749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.353C>T |
| AA Mutation | p.Ala118Val(p.A118V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285018 |
| Start | 13854555:13854555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.547C>T |
| AA Mutation | p.His183Tyr(p.H183Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285018 |
| Start | 13875095:13875095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201623293 |
| CDS Mutation | c.150G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285018 |
| Start | 13819382:13819382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs553027561 |
| CDS Mutation | c.612C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285018 |
| Start | 13819034:13819034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.960C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |