PDS5A
PDS5 cohesin associated factor A
Summary
The protein encoded by this gene binds to the cohesin complex and associates with chromatin through most of the cell cycle. The encoded protein may play a role in regulating sister chromatid cohesion during mitosis. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs769446864 | 4:39,839,628 | A/C | — | uncertain significance |
| rs2475052363 | 4:39,839,657 | C/G | — | uncertain significance |
| rs2475052370 | 4:39,839,659 | G/C | — | uncertain significance |
| rs780111750 | 4:39,839,728 | G/C | — | uncertain significance |
| rs177529 | 4:39,841,156 | T/C | intron variant | — |
| rs1322237156 | 4:39,846,394 | C/T | — | uncertain significance |
| rs1356331360 | 4:39,846,420 | G/A | — | uncertain significance |
| rs199515831 | 4:39,850,529 | T/C | — | uncertain significance |
| rs2475090059 | 4:39,850,550 | T/C | — | uncertain significance |
| rs1717875731 | 4:39,850,559 | C/T | — | uncertain significance |
| rs2475090117 | 4:39,850,562 | A/C | — | uncertain significance |
| rs747862865 | 4:39,851,216 | G/T | — | uncertain significance |
| rs753940583 | 4:39,864,509 | T/C | — | uncertain significance |
| rs1560435978 | 4:39,864,651 | G/A | — | uncertain significance |
| rs2475131000 | 4:39,865,074 | G/C | — | uncertain significance |
| rs2475140914 | 4:39,868,564 | C/A | — | uncertain significance |
| rs549448872 | 4:39,868,608 | T/C | — | uncertain significance |
| rs962415648 | 4:39,871,025 | C/T | — | uncertain significance |
| rs2475149792 | 4:39,871,041 | T/G | — | uncertain significance |
| rs368105443 | 4:39,874,659 | T/C | — | uncertain significance |
| rs904452984 | 4:39,874,721 | A/T | — | uncertain significance |
| rs1560445171 | 4:39,875,911 | C/A | — | uncertain significance |
| rs1720512441 | 4:39,878,612 | C/T | — | likely benign |
| rs2475173068 | 4:39,878,773 | C/T | — | uncertain significance |
| rs2475249758 | 4:39,900,134 | G/A | — | uncertain significance |
| rs1479888355 | 4:39,900,403 | T/C | — | uncertain significance |
| rs746888611 | 4:39,904,064 | T/C | — | uncertain significance |
| rs1360072840 | 4:39,915,318 | A/G | — | uncertain significance |
| rs2529672599 | 4:39,918,692 | C/T | — | uncertain significance |
| rs1195682087 | 4:39,921,959 | T/C | — | uncertain significance |
| rs377653620 | 4:39,921,981 | T/C | — | likely benign |
| rs1560486344 | 4:39,924,237 | C/G | — | uncertain significance |
| rs757396214 | 4:39,924,295 | C/T | — | uncertain significance |
| rs1725411279 | 4:39,927,526 | T/C | — | uncertain significance |
| rs369934532 | 4:39,929,597 | G/C | — | uncertain significance |
| rs75827282 | 4:39,949,846 | A/G | — | — |
| rs187673603 | 4:39,952,292 | C/A | intron variant | — |
| rs11733034 | 4:39,973,053 | G/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.