Primary Site >> Stomach Cancer
Gene >> PHF12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332830 |
| Start | 28924112:28924112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.512C>T |
| AA Mutation | p.Ala171Val(p.A171V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332830 |
| Start | 28921713:28921713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758095952 |
| CDS Mutation | c.811G>A |
| AA Mutation | p.Val271Ile(p.V271I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332830 |
| Start | 28912782:28912782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1789A>G |
| AA Mutation | p.Thr597Ala(p.T597A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332830 |
| Start | 28906491:28906491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377230866 |
| CDS Mutation | c.2707G>A |
| AA Mutation | p.Glu903Lys(p.E903K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332830 |
| Start | 28907602:28907602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2529A>G |
| AA Mutation | p.Ile843Met(p.I843M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332830 |
| Start | 28912880:28912880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753213832 |
| CDS Mutation | c.1691G>A |
| AA Mutation | p.Arg564Gln(p.R564Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332830 |
| Start | 28921696:28921696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.828G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332830 |
| Start | 28910275:28910275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751868565 |
| CDS Mutation | c.2310G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332830 |
| Start | 28912777:28912777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774066744 |
| CDS Mutation | c.1794C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332830 |
| Start | 28906884:28906884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2652T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332830 |
| Start | 28912993:28912993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147697011 |
| CDS Mutation | c.1578G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332830 |
| Start | 28910317:28910317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2268G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332830 |
| Start | 28911221:28911221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143319936 |
| CDS Mutation | c.2106C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |