RBM47
RNA binding motif protein 47
Summary
Enables enzyme binding activity; enzyme-substrate adaptor activity; and mRNA 3'-UTR binding activity. Involved in cytidine to uridine editing; positive regulation of type I interferon-mediated signaling pathway; and regulation of mRNA metabolic process. Located in cytoplasm and nucleus. Part of apolipoprotein B mRNA editing enzyme complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs781251500 | 4:40,427,938 | C/A | — | uncertain significance |
| rs2531317690 | 4:40,427,943 | G/A | — | uncertain significance |
| rs140354506 | 4:40,427,971 | G/A | — | uncertain significance |
| rs777559788 | 4:40,427,977 | C/T | — | uncertain significance |
| rs772534722 | 4:40,428,029 | G/T | — | uncertain significance |
| rs35529250 | 4:40,428,091 | C/T | missense variant | Likely benign |
| rs747609461 | 4:40,428,093 | T/C | — | uncertain significance |
| rs2531328850 | 4:40,428,139 | A/G | — | uncertain significance |
| rs142691111 | 4:40,428,151 | T/C | — | uncertain significance |
| rs146911971 | 4:40,434,684 | G/A | — | uncertain significance |
| rs780785396 | 4:40,434,712 | C/T | — | uncertain significance |
| rs1285642269 | 4:40,434,720 | G/A | — | uncertain significance |
| rs938475554 | 4:40,434,726 | G/A | — | uncertain significance |
| rs749771006 | 4:40,434,727 | C/T | — | uncertain significance |
| rs773506304 | 4:40,434,736 | C/T | — | uncertain significance |
| rs767171365 | 4:40,434,765 | A/G | — | uncertain significance |
| rs371309796 | 4:40,434,772 | T/C | — | uncertain significance |
| rs1299842507 | 4:40,434,774 | G/T | — | uncertain significance |
| rs1711558394 | 4:40,434,861 | C/G | — | uncertain significance |
| rs34196855 | 4:40,434,863 | A/G | — | benign |
| rs376009614 | 4:40,434,864 | A/T | — | uncertain significance |
| rs200872426 | 4:40,438,488 | C/T | — | uncertain significance |
| rs199905725 | 4:40,438,554 | G/T | — | uncertain significance |
| rs2531651563 | 4:40,438,557 | A/G | — | uncertain significance |
| rs773627724 | 4:40,439,893 | C/T | — | uncertain significance |
| rs537345346 | 4:40,439,904 | G/T | — | uncertain significance |
| rs766350310 | 4:40,439,935 | G/A | — | uncertain significance |
| rs1457668219 | 4:40,440,001 | T/C | — | uncertain significance |
| rs777068193 | 4:40,440,006 | T/C | — | uncertain significance |
| rs2531755286 | 4:40,440,211 | C/T | — | uncertain significance |
| rs2531757227 | 4:40,440,252 | T/A | — | uncertain significance |
| rs2531759859 | 4:40,440,304 | T/C | — | uncertain significance |
| rs2531764430 | 4:40,440,370 | C/A | — | uncertain significance |
| rs374159101 | 4:40,440,381 | C/T | — | uncertain significance |
| rs2531766220 | 4:40,440,402 | T/C | — | uncertain significance |
| rs62639979 | 4:40,440,552 | T/A | — | uncertain significance |
| rs2531781106 | 4:40,440,634 | C/T | — | likely benign |
| rs2531786557 | 4:40,440,722 | C/G | — | uncertain significance |
| rs201391084 | 4:40,440,783 | C/T | — | uncertain significance |
| rs2531791672 | 4:40,440,798 | A/G | — | uncertain significance |
| rs779921202 | 4:40,440,865 | C/A | — | uncertain significance |
| rs566403614 | 4:40,495,730 | G/A | — | — |
| rs10938226 | 4:40,562,644 | A/T | intron variant | — |
| rs547545693 | 4:40,579,986 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.