WAPL
WAPL cohesin release factor
Summary
Enables ATP-dependent protein-DNA unloader activity. Involved in several processes, including negative regulation of DNA replication; negative regulation of sister chromatid cohesion; and protein localization to chromatin. Located in several cellular components, including intercellular bridge; mitotic spindle; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs779088020 | 10:88,203,081 | A/G | — | uncertain significance |
| rs145776911 | 10:88,206,141 | A/T | — | uncertain significance |
| rs113314659 | 10:88,206,188 | G/A | — | uncertain significance |
| rs149475817 | 10:88,211,758 | C/T | — | uncertain significance |
| rs761768393 | 10:88,211,777 | C/T | — | uncertain significance |
| rs759906452 | 10:88,211,794 | A/G | — | uncertain significance |
| rs747049495 | 10:88,211,795 | T/C | — | uncertain significance |
| rs754307691 | 10:88,211,815 | G/C | — | uncertain significance |
| rs779199618 | 10:88,211,825 | T/C | — | uncertain significance |
| rs2492476116 | 10:88,211,827 | T/C | — | uncertain significance |
| rs368098376 | 10:88,213,482 | C/A | — | uncertain significance |
| rs1469974411 | 10:88,213,547 | C/T | — | uncertain significance |
| rs549492250 | 10:88,214,021 | A/G | — | — |
| rs7075426 | 10:88,216,402 | G/A | intron variant | — |
| rs754801490 | 10:88,220,207 | T/A | — | uncertain significance |
| rs576511427 | 10:88,221,622 | T/C | — | — |
| rs1564570621 | 10:88,227,214 | C/T | — | uncertain significance |
| rs2492523023 | 10:88,231,975 | G/A | — | uncertain significance |
| rs766612134 | 10:88,232,431 | T/C | — | uncertain significance |
| rs756172650 | 10:88,232,494 | G/T | — | uncertain significance |
| rs188548451 | 10:88,242,752 | G/A | intron variant | — |
| rs199670193 | 10:88,257,020 | T/C | — | uncertain significance |
| rs2492576417 | 10:88,257,056 | C/G | — | uncertain significance |
| rs754049466 | 10:88,259,481 | T/C | — | uncertain significance |
| rs2492580514 | 10:88,259,497 | A/C | — | uncertain significance |
| rs766280052 | 10:88,259,529 | G/T | — | uncertain significance |
| rs767272875 | 10:88,259,543 | G/A | — | uncertain significance |
| rs140697784 | 10:88,259,561 | G/T | — | uncertain significance |
| rs2492580842 | 10:88,259,562 | T/C | — | uncertain significance |
| rs946202472 | 10:88,259,580 | T/G | — | uncertain significance |
| rs2492581576 | 10:88,259,700 | G/T | — | uncertain significance |
| rs2492581649 | 10:88,259,730 | C/T | — | uncertain significance |
| rs765479869 | 10:88,259,756 | G/A | — | uncertain significance |
| rs745869394 | 10:88,259,848 | G/C | — | uncertain significance |
| rs1262112082 | 10:88,259,864 | C/T | — | uncertain significance |
| rs780074825 | 10:88,259,991 | C/T | — | uncertain significance |
| rs749589161 | 10:88,260,014 | G/A | — | uncertain significance |
| rs1842222151 | 10:88,260,018 | C/T | — | uncertain significance |
| rs759692026 | 10:88,260,044 | C/A | — | uncertain significance |
| rs776075411 | 10:88,260,051 | C/T | — | uncertain significance |
| rs138448848 | 10:88,260,150 | C/T | — | uncertain significance |
| rs777416367 | 10:88,260,260 | C/G | — | uncertain significance |
| rs267602601 | 10:88,260,362 | G/A | — | uncertain significance |
| rs1013786030 | 10:88,260,371 | G/C | — | uncertain significance |
| rs1046143626 | 10:88,260,390 | T/C | — | uncertain significance |
| rs143702248 | 10:88,260,464 | T/C | — | uncertain significance |
| rs1174057161 | 10:88,260,492 | C/G | — | uncertain significance |
| rs756161333 | 10:88,277,418 | C/T | — | uncertain significance |
| rs142162405 | 10:88,277,442 | C/G | — | uncertain significance |
| rs2492617816 | 10:88,277,585 | G/T | — | uncertain significance |
| rs149203854 | 10:88,277,664 | T/C | — | uncertain significance |
| rs770833625 | 10:88,277,760 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.