PHF20L1
PHD finger protein 20 like 1
Summary
Enables methylation-dependent protein binding activity. Involved in negative regulation of proteasomal ubiquitin-dependent protein catabolic process. Predicted to be located in nucleoplasm. Predicted to be part of NSL complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2488667324 | 8:133,790,117 | A/T | — | uncertain significance |
| rs6471099 | 8:133,792,740 | A/T | intron variant | — |
| rs761985134 | 8:133,806,718 | G/A | — | uncertain significance |
| rs762790733 | 8:133,807,055 | A/G | — | uncertain significance |
| rs745316202 | 8:133,811,047 | G/A | — | uncertain significance |
| rs151044859 | 8:133,811,074 | A/G | — | uncertain significance |
| rs2488928874 | 8:133,816,121 | A/G | — | uncertain significance |
| rs376961005 | 8:133,816,248 | A/G | — | uncertain significance |
| rs148199331 | 8:133,816,912 | A/G | — | benign |
| rs1254073286 | 8:133,826,966 | T/C | — | uncertain significance |
| rs780399495 | 8:133,827,083 | G/A | — | uncertain significance |
| rs761183001 | 8:133,829,181 | G/A | — | uncertain significance |
| rs2489085538 | 8:133,829,277 | T/C | — | uncertain significance |
| rs2489090589 | 8:133,829,593 | T/C | — | uncertain significance |
| rs1247715852 | 8:133,829,661 | A/G | — | uncertain significance |
| rs375482501 | 8:133,836,255 | C/T | — | uncertain significance |
| rs1307387788 | 8:133,837,517 | A/G | — | uncertain significance |
| rs202207817 | 8:133,837,554 | A/G | — | uncertain significance |
| rs771267278 | 8:133,837,614 | A/T | — | uncertain significance |
| rs777431336 | 8:133,844,500 | A/G | — | uncertain significance |
| rs1388662884 | 8:133,844,574 | C/G | — | uncertain significance |
| rs117764941 | 8:133,848,532 | G/A | downstream gene variant | — |
| rs75143612 | 8:133,849,655 | G/C | downstream gene variant | — |
| rs767807835 | 8:133,850,045 | G/A | — | uncertain significance |
| rs778303734 | 8:133,854,770 | C/T | — | uncertain significance |
| rs2489315149 | 8:133,854,785 | C/T | — | uncertain significance |
| rs913093438 | 8:133,854,926 | A/G | — | uncertain significance |
| rs945933106 | 8:133,854,930 | A/G | — | uncertain significance |
| rs1838058514 | 8:133,854,988 | C/G | — | uncertain significance |
| rs750338637 | 8:133,855,011 | G/T | — | uncertain significance |
| rs755995142 | 8:133,855,032 | T/C | — | uncertain significance |
| rs777077012 | 8:133,855,113 | C/G | — | uncertain significance |
| rs2489317953 | 8:133,855,115 | G/C | — | uncertain significance |
| rs765008775 | 8:133,856,462 | G/C | — | uncertain significance |
| rs371584027 | 8:133,856,557 | G/A | — | uncertain significance |
| rs2489346859 | 8:133,858,115 | C/G | — | uncertain significance |
| rs1336146117 | 8:133,858,148 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.