RAD54L2
RAD54 like 2
Summary
Predicted to enable ATP-dependent chromatin remodeler activity; protein kinase binding activity; and transcription coregulator activity. Predicted to be involved in chromatin organization. Predicted to act upstream of or within positive regulation of transcription by RNA polymerase II. Predicted to be located in nuclear speck. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants80 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs115266764 | 3:51,587,140 | A/C | — | — |
| rs576501736 | 3:51,608,986 | T/A | — | — |
| rs1408350580 | 3:51,624,527 | G/A | — | uncertain significance |
| rs4317086 | 3:51,652,016 | T/G | — | — |
| rs186743098 | 3:51,661,631 | C/T | — | uncertain significance |
| rs2470786559 | 3:51,661,683 | T/C | — | uncertain significance |
| rs565205386 | 3:51,661,689 | G/A | — | likely benign |
| rs113971604 | 3:51,661,777 | T/C | — | benign |
| rs1438802996 | 3:51,663,360 | C/T | — | uncertain significance |
| rs949793333 | 3:51,663,363 | G/C | — | uncertain significance |
| rs370856983 | 3:51,663,453 | G/A | — | uncertain significance |
| rs2470792089 | 3:51,664,353 | A/G | — | uncertain significance |
| rs778445151 | 3:51,664,762 | A/G | — | uncertain significance |
| rs148878049 | 3:51,664,847 | G/A | — | uncertain significance |
| rs2470798871 | 3:51,667,604 | C/G | — | uncertain significance |
| rs148593384 | 3:51,667,967 | C/T | — | uncertain significance |
| rs114438035 | 3:51,667,982 | C/T | — | uncertain significance |
| rs1203302993 | 3:51,667,987 | G/A | — | uncertain significance |
| rs770258894 | 3:51,667,992 | C/G | — | uncertain significance |
| rs1700915414 | 3:51,668,033 | T/C | — | uncertain significance |
| rs771939905 | 3:51,669,611 | C/T | — | uncertain significance |
| rs2470802679 | 3:51,669,613 | A/G | — | uncertain significance |
| rs2470802849 | 3:51,669,683 | T/G | — | uncertain significance |
| rs144719978 | 3:51,671,256 | C/G | — | benign |
| rs1300095829 | 3:51,671,386 | C/T | — | uncertain significance |
| rs144473707 | 3:51,671,458 | G/A | — | uncertain significance |
| rs774574331 | 3:51,671,461 | C/T | — | uncertain significance |
| rs1701034245 | 3:51,672,173 | G/C | — | uncertain significance |
| rs147665933 | 3:51,672,190 | C/T | — | benign |
| rs112749931 | 3:51,672,241 | A/G | — | benign |
| rs371166109 | 3:51,672,278 | T/C | — | uncertain significance |
| rs777257233 | 3:51,673,540 | C/T | — | uncertain significance |
| rs374021686 | 3:51,673,549 | C/T | — | likely benign |
| rs902915226 | 3:51,673,598 | T/C | — | uncertain significance |
| rs372073875 | 3:51,673,630 | G/A | — | uncertain significance |
| rs760340967 | 3:51,673,667 | A/G | — | uncertain significance |
| rs762831713 | 3:51,673,915 | A/G | — | uncertain significance |
| rs2470811620 | 3:51,673,933 | C/G | — | uncertain significance |
| rs749027629 | 3:51,675,838 | G/A | — | uncertain significance |
| rs2470815541 | 3:51,675,858 | G/T | — | uncertain significance |
| rs1029193941 | 3:51,677,957 | A/C | — | uncertain significance |
| rs2470822586 | 3:51,679,634 | T/C | — | uncertain significance |
| rs139803559 | 3:51,679,640 | A/G | — | uncertain significance |
| rs150924278 | 3:51,680,315 | T/C | — | benign |
| rs1393059415 | 3:51,680,347 | A/G | — | uncertain significance |
| rs1701278668 | 3:51,680,369 | A/T | — | uncertain significance |
| rs1463503723 | 3:51,680,428 | C/T | — | uncertain significance |
| rs772918692 | 3:51,680,454 | G/A | — | uncertain significance |
| rs143819415 | 3:51,680,478 | G/A | — | uncertain significance |
| rs1299629494 | 3:51,689,994 | A/G | — | uncertain significance |
| rs767939056 | 3:51,690,003 | G/A | — | likely benign |
| rs770556014 | 3:51,690,066 | C/T | — | uncertain significance |
| rs2470840862 | 3:51,690,085 | G/C | — | uncertain significance |
| rs894369801 | 3:51,690,090 | G/C | — | uncertain significance |
| rs201175331 | 3:51,690,111 | A/C | — | uncertain significance |
| rs763516756 | 3:51,694,045 | C/T | — | uncertain significance |
| rs747078994 | 3:51,694,098 | C/T | — | uncertain significance |
| rs185222323 | 3:51,694,120 | G/A | — | uncertain significance |
| rs142797468 | 3:51,696,501 | A/G | — | uncertain significance |
| rs111597009 | 3:51,696,509 | C/T | — | benign |
| rs755429540 | 3:51,696,534 | G/A | — | uncertain significance |
| rs376762989 | 3:51,696,538 | C/T | — | uncertain significance |
| rs759087593 | 3:51,696,598 | G/A | — | uncertain significance |
| rs564540485 | 3:51,696,607 | G/A | — | likely benign |
| rs184707777 | 3:51,696,668 | C/G | — | uncertain significance |
| rs748731842 | 3:51,696,681 | G/A | — | uncertain significance |
| rs755153740 | 3:51,696,697 | C/A | — | uncertain significance |
| rs139053490 | 3:51,696,840 | C/T | — | uncertain significance |
| rs781525636 | 3:51,696,868 | C/T | — | likely benign |
| rs754407997 | 3:51,696,873 | G/A | — | uncertain significance |
| rs938327194 | 3:51,696,880 | C/T | — | uncertain significance |
| rs894951879 | 3:51,696,937 | A/G | — | uncertain significance |
| rs1466889403 | 3:51,697,009 | A/G | — | uncertain significance |
| rs557480135 | 3:51,697,203 | C/A | — | uncertain significance |
| rs141079698 | 3:51,697,254 | A/G | — | uncertain significance |
| rs138986583 | 3:51,697,261 | C/T | — | uncertain significance |
| rs771221945 | 3:51,697,264 | G/A | — | uncertain significance |
| rs755846601 | 3:51,697,305 | G/A | — | uncertain significance |
| rs148251727 | 3:51,697,329 | C/T | — | uncertain significance |
| rs766992758 | 3:51,697,387 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.