RRP1B
ribosomal RNA processing 1B
Summary
Enables transcription coactivator activity. Involved in cellular response to virus; positive regulation of apoptotic process; and positive regulation of transcription by RNA polymerase II. Located in chromosome; granular component; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs531157051 | 21:45,079,631 | A/G | — | likely benign |
| rs9977076 | 21:45,085,829 | G/A | intron variant | — |
| rs201197840 | 21:45,089,776 | C/G | — | uncertain significance |
| rs11702544 | 21:45,091,861 | C/T | regulatory region variant | — |
| rs115629605 | 21:45,092,221 | C/T | — | benign |
| rs550211338 | 21:45,092,241 | C/T | — | conflicting classifications of pathogenicity |
| rs754525136 | 21:45,093,822 | G/A | — | uncertain significance |
| rs114577524 | 21:45,094,509 | T/A | — | benign |
| rs1284324188 | 21:45,094,559 | C/G | — | uncertain significance |
| rs1313799906 | 21:45,096,640 | G/A | — | uncertain significance |
| rs770600078 | 21:45,096,691 | C/T | — | uncertain significance |
| rs2516952992 | 21:45,096,747 | C/A | — | uncertain significance |
| rs779110819 | 21:45,096,771 | A/G | — | uncertain significance |
| rs747996554 | 21:45,103,205 | G/A | — | uncertain significance |
| rs369172517 | 21:45,104,510 | G/A | — | uncertain significance |
| rs757059637 | 21:45,104,527 | A/C | — | uncertain significance |
| rs948879084 | 21:45,105,658 | G/T | — | uncertain significance |
| rs142273251 | 21:45,106,740 | C/A | — | uncertain significance |
| rs776763861 | 21:45,107,471 | A/C | — | uncertain significance |
| rs1475879421 | 21:45,107,496 | C/G | — | uncertain significance |
| rs770776165 | 21:45,107,561 | C/G | — | uncertain significance |
| rs9306160 | 21:45,107,562 | T/A | missense variant | — |
| rs768645995 | 21:45,107,675 | C/T | — | uncertain significance |
| rs761894254 | 21:45,107,681 | C/T | — | uncertain significance |
| rs532710277 | 21:45,107,727 | T/C | — | likely benign |
| rs745358182 | 21:45,107,735 | C/G | — | uncertain significance |
| rs1369215788 | 21:45,107,804 | G/A | — | uncertain significance |
| rs911202990 | 21:45,107,805 | G/A | — | uncertain significance |
| rs2147175767 | 21:45,107,812 | A/G | — | likely benign |
| rs764628626 | 21:45,107,828 | C/T | — | uncertain significance |
| rs745909623 | 21:45,107,948 | C/A | — | uncertain significance |
| rs150022721 | 21:45,108,052 | G/C | — | uncertain significance |
| rs142322037 | 21:45,108,098 | G/A | — | uncertain significance |
| rs61737068 | 21:45,110,194 | T/C | — | benign |
| rs2083081604 | 21:45,110,220 | A/G | — | uncertain significance |
| rs141468438 | 21:45,110,253 | C/G | — | uncertain significance |
| rs777963278 | 21:45,110,296 | C/T | — | uncertain significance |
| rs746323090 | 21:45,110,313 | G/T | — | uncertain significance |
| rs148046281 | 21:45,111,329 | A/G | — | uncertain significance |
| rs766798880 | 21:45,113,110 | C/T | — | uncertain significance |
| rs377192517 | 21:45,113,133 | G/A | — | likely benign |
| rs2516964249 | 21:45,113,180 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.