Primary Site >> Stomach Cancer
Gene >> UCK1
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000372215 |
| Start | 131529584:131529584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.269A>T |
| AA Mutation | p.Asp90Val(p.D90V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372215 |
| Start | 131530569:131530569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.185T>C |
| AA Mutation | p.Leu62Pro(p.L62P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372215 |
| Start | 131530524:131530524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776397212 |
| CDS Mutation | c.230C>T |
| AA Mutation | p.Ala77Val(p.A77V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372215 |
| Start | 131525191:131525191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.683A>G |
| AA Mutation | p.Gln228Arg(p.Q228R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372215 |
| Start | 131530490:131530490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.264T>A |
| AA Mutation | p.His88Gln(p.H88Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372215 |
| Start | 131529156:131529156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149130090 |
| CDS Mutation | c.480C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372215 |
| Start | 131529165:131529165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746443101 |
| CDS Mutation | c.471C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |