RPAP3
RNA polymerase II associated protein 3
Summary
This gene encodes an RNA polymerase II-associated protein. The encoded protein may function in transcriptional regulation and may also regulate apoptosis. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs780726964 | 12:48,057,326 | T/C | — | uncertain significance |
| rs2539542759 | 12:48,060,810 | T/C | — | likely benign |
| rs758733529 | 12:48,060,811 | T/C | — | uncertain significance |
| rs745940783 | 12:48,060,820 | A/G | — | uncertain significance |
| rs371153105 | 12:48,061,598 | T/C | — | uncertain significance |
| rs1592467833 | 12:48,062,716 | A/C | — | uncertain significance |
| rs2539545442 | 12:48,062,727 | G/C | — | uncertain significance |
| rs1250910308 | 12:48,062,759 | C/A | — | uncertain significance |
| rs138253744 | 12:48,062,784 | G/A | — | uncertain significance |
| rs199534990 | 12:48,062,844 | C/T | — | uncertain significance |
| rs2539545716 | 12:48,062,863 | C/T | — | uncertain significance |
| rs771417626 | 12:48,063,953 | G/A | — | uncertain significance |
| rs776870361 | 12:48,063,954 | T/G | — | uncertain significance |
| rs746174790 | 12:48,063,963 | G/A | — | uncertain significance |
| rs764521578 | 12:48,064,015 | A/C | — | uncertain significance |
| rs138605014 | 12:48,064,044 | G/A | — | uncertain significance |
| rs149293092 | 12:48,064,094 | C/T | — | uncertain significance |
| rs1250624007 | 12:48,064,107 | T/G | — | uncertain significance |
| rs368438367 | 12:48,064,110 | T/A | — | uncertain significance |
| rs934495973 | 12:48,073,287 | G/A | — | uncertain significance |
| rs1939182069 | 12:48,073,310 | T/G | — | uncertain significance |
| rs2539560966 | 12:48,075,561 | T/A | — | uncertain significance |
| rs144540934 | 12:48,080,627 | C/T | — | uncertain significance |
| rs774819368 | 12:48,081,661 | G/A | — | uncertain significance |
| rs140206815 | 12:48,083,854 | A/C | intron variant | — |
| rs1186463939 | 12:48,084,361 | C/G | — | uncertain significance |
| rs748274753 | 12:48,090,117 | C/T | — | uncertain significance |
| rs775355665 | 12:48,090,126 | T/A | — | uncertain significance |
| rs200770635 | 12:48,091,430 | C/T | — | uncertain significance |
| rs200075662 | 12:48,091,448 | G/C | — | uncertain significance |
| rs151225713 | 12:48,091,454 | G/C | — | likely benign |
| rs994992515 | 12:48,091,471 | T/C | — | uncertain significance |
| rs150350108 | 12:48,091,473 | G/T | — | likely benign |
| rs138031379 | 12:48,091,499 | G/A | — | uncertain significance |
| rs200333932 | 12:48,095,330 | C/G | — | uncertain significance |
| rs1044795496 | 12:48,096,526 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.