PNRC1
proline rich nuclear receptor coactivator 1
Summary
Predicted to be involved in nuclear-transcribed mRNA catabolic process, nonsense-mediated decay. Predicted to be active in P-body and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2231265 | 6:89,790,201 | A/T | coding sequence variant | — |
| rs1385494375 | 6:89,790,637 | G/C | — | uncertain significance |
| rs147772027 | 6:89,790,650 | G/C | — | uncertain significance |
| rs2533261993 | 6:89,790,651 | T/A | — | uncertain significance |
| rs761772180 | 6:89,790,675 | T/C | — | uncertain significance |
| rs754598018 | 6:89,790,716 | G/A | — | uncertain significance |
| rs372473933 | 6:89,790,725 | G/A | — | uncertain significance |
| rs574722768 | 6:89,790,821 | C/G | — | uncertain significance |
| rs905666004 | 6:89,790,822 | C/G | — | uncertain significance |
| rs2533262537 | 6:89,790,826 | G/T | — | uncertain significance |
| rs758756337 | 6:89,790,879 | C/A | — | uncertain significance |
| rs780308921 | 6:89,790,881 | C/T | — | uncertain significance |
| rs945758138 | 6:89,790,899 | A/C | — | uncertain significance |
| rs1041462593 | 6:89,790,900 | A/G | — | uncertain significance |
| rs904285031 | 6:89,790,920 | C/T | — | uncertain significance |
| rs370418048 | 6:89,790,926 | A/G | — | uncertain significance |
| rs755200385 | 6:89,790,933 | C/G | — | uncertain significance |
| rs1391126540 | 6:89,790,941 | C/A | — | uncertain significance |
| rs760514591 | 6:89,790,983 | C/G | — | uncertain significance |
| rs768267668 | 6:89,790,984 | T/C | — | uncertain significance |
| rs761299659 | 6:89,790,989 | G/T | — | uncertain significance |
| rs917888226 | 6:89,791,041 | C/T | — | uncertain significance |
| rs1438569879 | 6:89,791,070 | G/A | — | uncertain significance |
| rs1006303852 | 6:89,791,109 | C/T | — | uncertain significance |
| rs1016931112 | 6:89,791,142 | C/T | — | uncertain significance |
| rs2533269555 | 6:89,793,488 | T/C | — | uncertain significance |
| rs558286572 | 6:89,793,660 | C/G | — | uncertain significance |
| rs148749690 | 6:89,793,698 | C/T | — | uncertain significance |
| rs370470988 | 6:89,793,700 | G/A | — | uncertain significance |
| rs201429422 | 6:89,793,839 | G/A | — | uncertain significance |
| rs1130809 | 6:89,793,894 | G/T | synonymous variant | — |
| rs578015348 | 6:89,793,902 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.