Primary Site >> Stomach Cancer
Gene >> ZNF263
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219069 |
| Start | 3290004:3290004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1498G>A |
| AA Mutation | p.Ala500Thr(p.A500T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219069 |
| Start | 3289480:3289480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs79713839 |
| CDS Mutation | c.974G>A |
| AA Mutation | p.Arg325Gln(p.R325Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219069 |
| Start | 3290119:3290119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1613G>T |
| AA Mutation | p.Arg538Ile(p.R538I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219069 |
| Start | 3283852:3283852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.34G>T |
| AA Mutation | p.Gly12Trp(p.G12W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219069 |
| Start | 3284025:3284025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.207G>T |
| AA Mutation | p.Trp69Cys(p.W69C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219069 |
| Start | 3289732:3289732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1226T>C |
| AA Mutation | p.Val409Ala(p.V409A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219069 |
| Start | 3289723:3289723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1217G>A |
| AA Mutation | p.Cys406Tyr(p.C406Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219069 |
| Start | 3290259:3290259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138118006 |
| CDS Mutation | c.1753C>T |
| AA Mutation | p.Arg585Trp(p.R585W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |