Primary Site >> Stomach Cancer
Gene >> ZNF559
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393883 |
| Start | 9343021:9343021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1570T>G |
| AA Mutation | p.Cys524Gly(p.C524G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393883 |
| Start | 9341785:9341785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.334A>G |
| AA Mutation | p.Thr112Ala(p.T112A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393883 |
| Start | 9341888:9341888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.437T>G |
| AA Mutation | p.Leu146Arg(p.L146R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393883 |
| Start | 9339203:9339203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147865057 |
| CDS Mutation | c.44C>T |
| AA Mutation | p.Thr15Ile(p.T15I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393883 |
| Start | 9339284:9339284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.125T>C |
| AA Mutation | p.Val42Ala(p.V42A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393883 |
| Start | 9341147:9341147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.206A>T |
| AA Mutation | p.Asn69Ile(p.N69I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393883 |
| Start | 9342368:9342368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.917T>G |
| AA Mutation | p.Phe306Cys(p.F306C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393883 |
| Start | 9341878:9341878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772834767 |
| CDS Mutation | c.427G>A |
| AA Mutation | p.Gly143Arg(p.G143R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393883 |
| Start | 9341733:9341733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.282C>G |
| AA Mutation | p.Asn94Lys(p.N94K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393883 |
| Start | 9341877:9341877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147973414 |
| CDS Mutation | c.426C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |