Primary Site >> Stomach Cancer
Gene >> WNT3A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284523 |
| Start | 228022846:228022846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750564361 |
| CDS Mutation | c.251G>A |
| AA Mutation | p.Arg84His(p.R84H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284523 |
| Start | 228059034:228059034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.628G>A |
| AA Mutation | p.Gly210Ser(p.G210S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284523 |
| Start | 228058993:228058993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.587C>T |
| AA Mutation | p.Ala196Val(p.A196V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284523 |
| Start | 228050847:228050847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.505T>C |
| AA Mutation | p.Phe169Leu(p.F169L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284523 |
| Start | 228059181:228059181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.775C>T |
| AA Mutation | p.Arg259Cys(p.R259C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284523 |
| Start | 228059206:228059206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.800C>T |
| AA Mutation | p.Thr267Met(p.T267M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284523 |
| Start | 228050815:228050815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.473A>G |
| AA Mutation | p.Asp158Gly(p.D158G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284523 |
| Start | 228022772:228022772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745929272 |
| CDS Mutation | c.177C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |