RPAP1
RNA polymerase II associated protein 1
Summary
This protein forms part of the RNA polymerase II (RNAPII) enzyme complex and may recruit RNAPII to chromatin through its interaction with acetylated histones. [provided by RefSeq, Jul 2012]
Known Variants89 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs563339353 | 15:41,809,802 | G/A | — | uncertain significance |
| rs1418290690 | 15:41,809,811 | G/T | — | uncertain significance |
| rs1271704600 | 15:41,809,864 | T/C | — | uncertain significance |
| rs2051683516 | 15:41,810,247 | G/A | — | uncertain significance |
| rs764575533 | 15:41,810,280 | C/T | — | likely benign |
| rs369609807 | 15:41,810,292 | G/A | — | uncertain significance |
| rs184673233 | 15:41,812,834 | C/T | — | uncertain significance |
| rs758904972 | 15:41,812,858 | G/C | — | uncertain significance |
| rs1259315681 | 15:41,812,882 | C/T | — | uncertain significance |
| rs771893792 | 15:41,812,921 | G/A | — | uncertain significance |
| rs1282318051 | 15:41,812,936 | C/G | — | uncertain significance |
| rs372226785 | 15:41,812,957 | G/A | — | uncertain significance |
| rs768505568 | 15:41,813,023 | A/G | — | likely benign |
| rs774890309 | 15:41,813,047 | C/T | — | uncertain significance |
| rs767925586 | 15:41,813,049 | C/G | — | uncertain significance |
| rs377151806 | 15:41,813,061 | C/A | — | uncertain significance |
| rs7170898 | 15:41,813,062 | G/C | — | conflicting classifications of pathogenicity |
| rs754882833 | 15:41,813,086 | C/T | — | uncertain significance |
| rs748913456 | 15:41,813,106 | G/A | — | likely benign |
| rs201568853 | 15:41,813,206 | G/C | — | uncertain significance |
| rs1358404328 | 15:41,813,231 | G/T | — | uncertain significance |
| rs144376568 | 15:41,813,242 | C/T | — | uncertain significance |
| rs373430885 | 15:41,813,951 | C/T | — | uncertain significance |
| rs1482688868 | 15:41,814,030 | T/A | — | uncertain significance |
| rs778356661 | 15:41,814,074 | G/A | — | uncertain significance |
| rs764481480 | 15:41,814,345 | C/T | — | uncertain significance |
| rs770830559 | 15:41,814,397 | C/T | — | uncertain significance |
| rs147913656 | 15:41,814,409 | A/G | — | uncertain significance |
| rs2550223972 | 15:41,814,982 | T/G | — | uncertain significance |
| rs774703409 | 15:41,815,061 | G/A | — | uncertain significance |
| rs189977450 | 15:41,815,064 | G/A | — | uncertain significance |
| rs147507787 | 15:41,815,135 | G/A | — | uncertain significance |
| rs763634599 | 15:41,815,513 | G/A | — | uncertain significance |
| rs2051758073 | 15:41,815,983 | C/T | — | uncertain significance |
| rs780329861 | 15:41,815,995 | C/T | — | uncertain significance |
| rs369954246 | 15:41,816,072 | G/A | — | uncertain significance |
| rs768519207 | 15:41,816,139 | G/A | — | uncertain significance |
| rs2550224752 | 15:41,816,160 | C/T | — | uncertain significance |
| rs2550224912 | 15:41,816,363 | A/G | — | uncertain significance |
| rs766528527 | 15:41,816,408 | C/T | — | likely benign |
| rs545307017 | 15:41,816,409 | G/A | — | uncertain significance |
| rs371584065 | 15:41,817,247 | C/T | — | uncertain significance |
| rs139615608 | 15:41,817,312 | C/T | — | uncertain significance |
| rs144451437 | 15:41,817,313 | G/A | — | uncertain significance |
| rs777348644 | 15:41,817,321 | C/T | — | uncertain significance |
| rs560065091 | 15:41,819,254 | G/A | — | uncertain significance |
| rs995978971 | 15:41,819,256 | C/T | — | uncertain significance |
| rs762136187 | 15:41,819,391 | G/A | — | uncertain significance |
| rs140704516 | 15:41,819,432 | G/A | — | uncertain significance |
| rs1343749236 | 15:41,819,438 | C/G | — | uncertain significance |
| rs764215280 | 15:41,819,472 | G/A | — | uncertain significance |
| rs1270610625 | 15:41,819,662 | T/C | — | uncertain significance |
| rs1414043283 | 15:41,819,663 | T/G | — | uncertain significance |
| rs745455889 | 15:41,819,664 | T/G | — | uncertain significance |
| rs137979437 | 15:41,819,772 | T/C | — | uncertain significance |
| rs779826774 | 15:41,819,794 | C/T | — | uncertain significance |
| rs752342210 | 15:41,820,201 | G/A | — | uncertain significance |
| rs2051813026 | 15:41,820,203 | T/C | — | uncertain significance |
| rs910417343 | 15:41,820,486 | C/T | — | uncertain significance |
| rs1332160471 | 15:41,820,495 | G/A | — | uncertain significance |
| rs762812209 | 15:41,820,530 | G/A | — | uncertain significance |
| rs190804095 | 15:41,821,718 | C/T | — | uncertain significance |
| rs767333147 | 15:41,823,244 | T/A | — | uncertain significance |
| rs2550227537 | 15:41,823,258 | C/A | — | uncertain significance |
| rs139766998 | 15:41,823,275 | A/T | — | uncertain significance |
| rs567280087 | 15:41,823,310 | G/A | — | uncertain significance |
| rs1338821820 | 15:41,823,344 | C/T | — | uncertain significance |
| rs752476338 | 15:41,823,350 | T/C | — | likely benign |
| rs201802698 | 15:41,823,361 | G/A | — | uncertain significance |
| rs2550228567 | 15:41,826,971 | A/G | — | uncertain significance |
| rs2051891889 | 15:41,827,058 | C/T | — | uncertain significance |
| rs140474963 | 15:41,827,060 | C/A | — | uncertain significance |
| rs2297381 | 15:41,827,655 | C/T | intron variant | — |
| rs760388308 | 15:41,827,737 | C/A | — | uncertain significance |
| rs148016359 | 15:41,827,745 | A/G | — | uncertain significance |
| rs990168268 | 15:41,828,343 | C/T | — | uncertain significance |
| rs368467030 | 15:41,828,380 | C/G | — | uncertain significance |
| rs143671800 | 15:41,828,392 | C/T | — | uncertain significance |
| rs376246565 | 15:41,828,711 | C/G | — | uncertain significance |
| rs1163329949 | 15:41,828,815 | A/G | — | uncertain significance |
| rs776842922 | 15:41,828,847 | T/C | — | uncertain significance |
| rs769976952 | 15:41,829,164 | G/A | — | uncertain significance |
| rs1309147821 | 15:41,829,203 | C/A | — | uncertain significance |
| rs565194955 | 15:41,829,223 | T/A | — | uncertain significance |
| rs2550229854 | 15:41,829,242 | G/A | — | uncertain significance |
| rs773385051 | 15:41,829,257 | C/G | — | uncertain significance |
| rs763915396 | 15:41,829,268 | C/T | — | uncertain significance |
| rs61731588 | 15:41,829,316 | G/A | — | benign |
| rs7163686 | 15:41,833,208 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.