RCL1
RNA terminal phosphate cyclase like 1
Summary
Predicted to enable RNA endonuclease activity. Involved in ribosomal small subunit biogenesis. Part of small-subunit processome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants59 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs183111502 | 9:4,791,687 | C/A | upstream gene variant | — |
| rs423955 | 9:4,792,339 | C/A | — | — |
| rs369962099 | 9:4,793,179 | G/C | — | uncertain significance |
| rs1035115030 | 9:4,793,188 | C/G | — | uncertain significance |
| rs184146494 | 9:4,799,990 | T/C | downstream gene variant | — |
| rs113884699 | 9:4,800,430 | G/A | — | — |
| rs182851782 | 9:4,801,994 | C/T | downstream gene variant | — |
| rs560950743 | 9:4,802,087 | T/A | — | — |
| rs10974792 | 9:4,803,442 | T/A | downstream gene variant | — |
| rs774207950 | 9:4,814,862 | G/A | — | — |
| rs13300663 | 9:4,814,948 | G/C | regulatory region variant | — |
| rs141139955 | 9:4,816,681 | G/C | intron variant | — |
| rs76742217 | 9:4,821,273 | G/A | intron variant | — |
| rs749214150 | 9:4,823,579 | C/A | — | uncertain significance |
| rs1275999363 | 9:4,823,587 | C/T | — | uncertain significance |
| rs115216700 | 9:4,823,599 | G/A | — | uncertain significance |
| rs1332555032 | 9:4,826,906 | A/C | — | uncertain significance |
| rs150920079 | 9:4,826,920 | G/A | — | uncertain significance |
| rs1460301381 | 9:4,826,926 | C/T | — | uncertain significance |
| rs374580393 | 9:4,826,927 | G/A | — | uncertain significance |
| rs138474156 | 9:4,827,014 | A/G | — | uncertain significance |
| rs1816786087 | 9:4,827,019 | C/T | — | pathogenic |
| rs199997829 | 9:4,827,763 | T/C | — | — |
| rs554625134 | 9:4,833,178 | C/T | — | uncertain significance |
| rs143996516 | 9:4,833,202 | A/C | — | uncertain significance |
| rs190434396 | 9:4,833,375 | C/G | regulatory region variant | — |
| rs116589736 | 9:4,834,150 | C/T | — | uncertain significance |
| rs457287 | 9:4,834,394 | A/G | regulatory region variant | — |
| rs1270231 | 9:4,840,877 | G/T | — | — |
| rs76643175 | 9:4,841,222 | C/T | — | benign |
| rs371417592 | 9:4,841,245 | G/A | — | uncertain significance |
| rs114500329 | 9:4,841,290 | A/C | — | uncertain significance |
| rs749243435 | 9:4,841,337 | G/C | — | uncertain significance |
| rs295260 | 9:4,842,773 | A/G | intron variant | — |
| rs7868737 | 9:4,843,672 | C/G | intron variant | — |
| rs2236496 | 9:4,844,265 | T/C | intron variant | — |
| rs1201302921 | 9:4,844,566 | G/A | — | likely benign |
| rs751699813 | 9:4,844,656 | G/A | — | uncertain significance |
| rs2236498 | 9:4,844,778 | A/T | — | — |
| rs10815094 | 9:4,845,520 | A/C | — | — |
| rs3824430 | 9:4,847,168 | T/A | — | — |
| rs7874244 | 9:4,847,570 | T/G | — | — |
| rs1255905866 | 9:4,849,463 | C/T | — | uncertain significance |
| rs35815255 | 9:4,849,515 | C/T | — | benign |
| rs2488666926 | 9:4,849,520 | A/G | — | uncertain significance |
| rs149023617 | 9:4,849,526 | T/C | — | uncertain significance |
| rs17803780 | 9:4,849,647 | T/C | regulatory region variant | — |
| rs456179 | 9:4,851,966 | C/A | — | — |
| rs76635833 | 9:4,852,605 | C/T | regulatory region variant | — |
| rs10758657 | 9:4,853,751 | A/G | downstream gene variant | — |
| rs10974817 | 9:4,856,417 | A/C | — | — |
| rs10758658 | 9:4,856,877 | G/A | downstream gene variant | — |
| rs10758659 | 9:4,858,019 | A/G | downstream gene variant | — |
| rs201249508 | 9:4,860,108 | A/T | upstream gene variant | — |
| rs142051884 | 9:4,860,138 | C/T | — | uncertain significance |
| rs370635863 | 9:4,860,160 | A/C | — | uncertain significance |
| rs763588238 | 9:4,860,186 | C/G | — | uncertain significance |
| rs368179527 | 9:4,860,189 | T/C | — | uncertain significance |
| rs2488681412 | 9:4,860,254 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.