Primary Site >> Stomach Cancer
Gene >> ZNF721
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338977 |
| Start | 443119:443119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1312T>C |
| AA Mutation | p.Cys438Arg(p.C438R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338977 |
| Start | 444211:444211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782442388 |
| CDS Mutation | c.220C>T |
| AA Mutation | p.Arg74Cys(p.R74C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338977 |
| Start | 442073:442073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2358A>C |
| AA Mutation | p.Lys786Asn(p.K786N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338977 |
| Start | 443409:443409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781992777 |
| CDS Mutation | c.1022G>T |
| AA Mutation | p.Arg341Ile(p.R341I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338977 |
| Start | 443997:443997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.434A>C |
| AA Mutation | p.Lys145Thr(p.K145T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338977 |
| Start | 442158:442158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2273G>T |
| AA Mutation | p.Arg758Ile(p.R758I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338977 |
| Start | 442695:442695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1736G>A |
| AA Mutation | p.Gly579Asp(p.G579D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338977 |
| Start | 441801:441801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2630G>A |
| AA Mutation | p.Gly877Glu(p.G877E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338977 |
| Start | 442218:442218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2213A>T |
| AA Mutation | p.Asp738Val(p.D738V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338977 |
| Start | 442516:442516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1915G>A |
| AA Mutation | p.Ala639Thr(p.A639T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338977 |
| Start | 443516:443516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368622788 |
| CDS Mutation | c.915C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338977 |
| Start | 442907:442907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1524G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338977 |
| Start | 444389:444389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.42G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338977 |
| Start | 443378:443378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375258970 |
| CDS Mutation | c.1053C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338977 |
| Start | 442517:442517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1914T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |