Primary Site >> Stomach Cancer
Gene >> WNT9B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290015 |
| Start | 46875128:46875128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375739988 |
| CDS Mutation | c.362C>T |
| AA Mutation | p.Ala121Val(p.A121V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290015 |
| Start | 46875328:46875328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.562G>A |
| AA Mutation | p.Ala188Thr(p.A188T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290015 |
| Start | 46875313:46875313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.547A>T |
| AA Mutation | p.Asn183Tyr(p.N183Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290015 |
| Start | 46875286:46875286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.520A>G |
| AA Mutation | p.Ser174Gly(p.S174G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290015 |
| Start | 46875280:46875280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.514T>C |
| AA Mutation | p.Phe172Leu(p.F172L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290015 |
| Start | 46872583:46872583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146743600 |
| CDS Mutation | c.144C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290015 |
| Start | 46872742:46872742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.303C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290015 |
| Start | 46876658:46876658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771046022 |
| CDS Mutation | c.1014C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290015 |
| Start | 46872655:46872655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs535771134 |
| CDS Mutation | c.216C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |