RRP1
ribosomal RNA processing 1
Summary
The protein encoded by this gene is the putative homolog of the yeast ribosomal RNA processing protein RRP1. The encoded protein is involved in the late stages of nucleologenesis at the end of mitosis, and may be required for the generation of 28S rRNA. [provided by RefSeq, Jul 2008]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs56227640 | 21:45,208,686 | T/G | regulatory region variant | — |
| rs774679026 | 21:45,209,569 | A/G | — | uncertain significance |
| rs759119620 | 21:45,209,591 | G/A | — | likely benign |
| rs766533429 | 21:45,211,258 | A/C | — | uncertain significance |
| rs774030035 | 21:45,211,292 | G/A | — | uncertain significance |
| rs184838512 | 21:45,213,190 | C/T | — | benign |
| rs768772947 | 21:45,213,216 | G/C | — | uncertain significance |
| rs760895439 | 21:45,213,248 | C/T | — | uncertain significance |
| rs763767114 | 21:45,213,265 | C/T | — | uncertain significance |
| rs1300965054 | 21:45,213,283 | A/G | — | uncertain significance |
| rs74925444 | 21:45,214,635 | G/A | intron variant | — |
| rs142644786 | 21:45,217,423 | C/T | — | likely benign |
| rs764549852 | 21:45,217,431 | A/C | — | uncertain significance |
| rs34224504 | 21:45,217,539 | A/T | — | uncertain significance |
| rs376009014 | 21:45,217,557 | A/G | — | uncertain significance |
| rs373040342 | 21:45,217,829 | C/T | — | uncertain significance |
| rs773617935 | 21:45,217,843 | G/T | — | uncertain significance |
| rs201075773 | 21:45,217,930 | G/A | — | uncertain significance |
| rs772909448 | 21:45,217,937 | G/C | — | uncertain significance |
| rs752763619 | 21:45,217,945 | G/A | — | likely benign |
| rs58028593 | 21:45,217,973 | C/T | — | benign |
| rs746385277 | 21:45,217,974 | G/A | — | likely benign |
| rs2517202261 | 21:45,219,454 | C/T | — | uncertain significance |
| rs144068997 | 21:45,219,455 | C/T | — | benign |
| rs766636330 | 21:45,219,501 | G/A | — | uncertain significance |
| rs563106945 | 21:45,219,520 | C/G | — | uncertain significance |
| rs769697557 | 21:45,219,522 | G/A | — | uncertain significance |
| rs373245016 | 21:45,220,443 | C/T | — | uncertain significance |
| rs376330937 | 21:45,220,491 | C/T | — | uncertain significance |
| rs768315459 | 21:45,222,196 | C/T | — | uncertain significance |
| rs200137494 | 21:45,222,214 | C/T | — | uncertain significance |
| rs200910420 | 21:45,222,239 | A/G | — | uncertain significance |
| rs772094375 | 21:45,222,242 | G/A | — | uncertain significance |
| rs201873899 | 21:45,222,254 | T/G | — | uncertain significance |
| rs75229405 | 21:45,223,383 | G/C | — | benign |
| rs368644724 | 21:45,223,395 | A/C | — | uncertain significance |
| rs374983239 | 21:45,223,470 | G/A | — | likely benign |
| rs371352025 | 21:45,223,477 | G/A | — | uncertain significance |
| rs1436172220 | 21:45,223,513 | G/A | — | uncertain significance |
| rs762121219 | 21:45,223,532 | G/C | — | uncertain significance |
| rs375793237 | 21:45,223,543 | G/A | — | uncertain significance |
| rs1283469182 | 21:45,223,549 | A/G | — | likely benign |
| rs2517208480 | 21:45,223,608 | G/T | — | uncertain significance |
| rs756760981 | 21:45,223,609 | C/T | — | likely benign |
| rs749255086 | 21:45,223,627 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.