Primary Site >> Stomach Cancer
Gene >> WNT5A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264634 |
| Start | 55470387:55470387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.848A>G |
| AA Mutation | p.Lys283Arg(p.K283R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264634 |
| Start | 55470429:55470429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.806A>C |
| AA Mutation | p.Lys269Thr(p.K269T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264634 |
| Start | 55470414:55470414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.821C>T |
| AA Mutation | p.Ala274Val(p.A274V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000264634 |
| Start | 55479563:55479563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.142T>C |
| AA Mutation | p.Ser48Pro(p.S48P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264634 |
| Start | 55470367:55470367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.868C>T |
| AA Mutation | p.Arg290Cys(p.R290C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264634 |
| Start | 55470289:55470289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.946G>A |
| AA Mutation | p.Gly316Ser(p.G316S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264634 |
| Start | 55470234:55470234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1001G>A |
| AA Mutation | p.Gly334Asp(p.G334D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264634 |
| Start | 55474410:55474410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.611G>A |
| AA Mutation | p.Arg204His(p.R204H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264634 |
| Start | 55479368:55479368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.337T>C |
| AA Mutation | p.Trp113Arg(p.W113R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264634 |
| Start | 55474391:55474391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.630C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264634 |
| Start | 55479393:55479393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.312C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264634 |
| Start | 55479414:55479414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762941459 |
| CDS Mutation | c.291G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |