Primary Site >> Stomach Cancer
Gene >> WNT5B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310594 |
| Start | 1639792:1639792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375865925 |
| CDS Mutation | c.437C>T |
| AA Mutation | p.Thr146Met(p.T146M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310594 |
| Start | 1639797:1639797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.442C>T |
| AA Mutation | p.Arg148Trp(p.R148W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310594 |
| Start | 1645926:1645926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763442249 |
| CDS Mutation | c.754G>A |
| AA Mutation | p.Ala252Thr(p.A252T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310594 |
| Start | 1639891:1639891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs190705769 |
| CDS Mutation | c.536G>A |
| AA Mutation | p.Arg179Gln(p.R179Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310594 |
| Start | 1645888:1645888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529807731 |
| CDS Mutation | c.716G>A |
| AA Mutation | p.Arg239His(p.R239H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310594 |
| Start | 1639757:1639757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.402C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310594 |
| Start | 1645814:1645814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756050341 |
| CDS Mutation | c.642C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |