RBM19
RNA binding motif protein 19
Summary
This gene encodes a nucleolar protein that contains six RNA-binding motifs. The encoded protein may be involved in regulating ribosome biogenesis. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Apr 2009]
Known Variants71 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs143207270 | 12:114,261,091 | C/T | — | uncertain significance |
| rs766739457 | 12:114,282,500 | G/A | — | uncertain significance |
| rs575444859 | 12:114,282,505 | G/C | — | uncertain significance |
| rs138017624 | 12:114,282,592 | C/T | — | uncertain significance |
| rs763813487 | 12:114,296,604 | C/G | — | uncertain significance |
| rs201331823 | 12:114,296,631 | C/T | — | uncertain significance |
| rs146110962 | 12:114,296,675 | C/T | — | uncertain significance |
| rs948426316 | 12:114,296,689 | C/G | — | uncertain significance |
| rs77531286 | 12:114,299,548 | T/C | regulatory region variant | — |
| rs3955311 | 12:114,343,818 | C/T | intron variant | — |
| rs767897536 | 12:114,352,800 | G/C | — | uncertain significance |
| rs148092321 | 12:114,352,822 | C/T | — | uncertain significance |
| rs150650047 | 12:114,352,860 | T/G | — | uncertain significance |
| rs369747435 | 12:114,352,883 | C/T | — | uncertain significance |
| rs200569958 | 12:114,356,206 | C/T | — | uncertain significance |
| rs574667329 | 12:114,356,225 | C/G | — | uncertain significance |
| rs368226146 | 12:114,356,246 | C/T | — | likely benign |
| rs763718755 | 12:114,358,493 | C/T | — | uncertain significance |
| rs3782455 | 12:114,359,265 | G/T | intron variant | — |
| rs543919031 | 12:114,363,981 | G/A | — | — |
| rs141407656 | 12:114,364,869 | T/G | — | likely benign |
| rs2541049032 | 12:114,364,918 | C/G | — | uncertain significance |
| rs776391021 | 12:114,364,927 | T/C | — | uncertain significance |
| rs2541049142 | 12:114,364,942 | C/T | — | uncertain significance |
| rs1869157943 | 12:114,364,948 | C/T | — | uncertain significance |
| rs538558405 | 12:114,365,023 | C/T | — | uncertain significance |
| rs370314715 | 12:114,374,856 | G/A | — | uncertain significance |
| rs1282787177 | 12:114,374,922 | T/G | — | uncertain significance |
| rs757063191 | 12:114,377,824 | C/A | — | uncertain significance |
| rs202108762 | 12:114,380,175 | C/T | — | uncertain significance |
| rs568147769 | 12:114,380,176 | G/A | — | uncertain significance |
| rs1428185567 | 12:114,380,182 | C/T | — | uncertain significance |
| rs767977845 | 12:114,380,224 | C/T | — | uncertain significance |
| rs145390142 | 12:114,381,974 | G/A | intron variant | — |
| rs554733672 | 12:114,383,661 | T/C | — | likely benign |
| rs200306327 | 12:114,383,683 | C/T | — | uncertain significance |
| rs201150757 | 12:114,383,723 | G/C | — | uncertain significance |
| rs756884154 | 12:114,384,180 | T/C | — | uncertain significance |
| rs1328850469 | 12:114,384,223 | T/C | — | uncertain significance |
| rs200023557 | 12:114,384,232 | C/T | — | uncertain significance |
| rs1361787741 | 12:114,384,246 | T/C | — | uncertain significance |
| rs150497537 | 12:114,384,268 | G/A | — | uncertain significance |
| rs80245977 | 12:114,385,245 | G/A | — | uncertain significance |
| rs369103042 | 12:114,385,248 | T/C | — | uncertain significance |
| rs746941474 | 12:114,386,741 | C/A | — | uncertain significance |
| rs375007299 | 12:114,386,806 | C/T | — | uncertain significance |
| rs369295504 | 12:114,386,827 | C/T | — | uncertain significance |
| rs149098977 | 12:114,386,832 | T/C | — | uncertain significance |
| rs199576221 | 12:114,387,899 | C/T | — | uncertain significance |
| rs763155552 | 12:114,387,954 | T/C | — | likely benign |
| rs377648094 | 12:114,392,952 | G/A | — | uncertain significance |
| rs200727713 | 12:114,392,997 | T/G | — | uncertain significance |
| rs200807760 | 12:114,395,682 | C/T | — | likely benign |
| rs767573998 | 12:114,395,734 | A/C | — | uncertain significance |
| rs775860918 | 12:114,395,775 | C/G | — | uncertain significance |
| rs1180855141 | 12:114,395,777 | T/C | — | uncertain significance |
| rs758124511 | 12:114,395,810 | G/A | — | uncertain significance |
| rs910138983 | 12:114,397,068 | A/C | — | uncertain significance |
| rs1278097205 | 12:114,397,070 | T/C | — | uncertain significance |
| rs1171789289 | 12:114,397,094 | G/A | — | uncertain significance |
| rs1872275480 | 12:114,397,124 | T/C | — | uncertain significance |
| rs139578414 | 12:114,397,197 | T/C | — | uncertain significance |
| rs149741620 | 12:114,397,678 | G/C | — | uncertain significance |
| rs762025832 | 12:114,397,691 | C/A | — | uncertain significance |
| rs146764943 | 12:114,397,888 | G/T | — | uncertain significance |
| rs1301817184 | 12:114,400,045 | G/A | — | uncertain significance |
| rs199537906 | 12:114,400,065 | T/C | — | likely benign |
| rs145566044 | 12:114,400,138 | T/C | — | uncertain significance |
| rs138583748 | 12:114,400,185 | G/A | — | uncertain significance |
| rs746173741 | 12:114,400,199 | C/A | — | uncertain significance |
| rs144104796 | 12:114,404,000 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.