VIRMA
vir like m6A methyltransferase associated
Summary
Enables RNA binding activity. Involved in mRNA processing. Located in RNA N6-methyladenosine methyltransferase complex; cytosol; and nuclear speck. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants68 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs776496785 | 8:95,501,071 | G/A | — | uncertain significance |
| rs200651420 | 8:95,501,082 | C/T | — | uncertain significance |
| rs762579896 | 8:95,502,191 | G/A | — | uncertain significance |
| rs147465632 | 8:95,502,257 | T/C | — | uncertain significance |
| rs568758321 | 8:95,503,814 | G/A | — | uncertain significance |
| rs745569493 | 8:95,503,821 | G/A | — | uncertain significance |
| rs1015632043 | 8:95,503,920 | G/A | — | uncertain significance |
| rs143106267 | 8:95,504,906 | G/T | — | uncertain significance |
| rs772231079 | 8:95,505,026 | T/G | — | uncertain significance |
| rs763006732 | 8:95,507,176 | T/C | — | uncertain significance |
| rs566504056 | 8:95,508,019 | T/A | — | uncertain significance |
| rs367623928 | 8:95,508,022 | C/T | — | uncertain significance |
| rs2488065386 | 8:95,508,080 | C/T | — | uncertain significance |
| rs1314322959 | 8:95,508,651 | T/C | — | uncertain significance |
| rs368083067 | 8:95,508,692 | T/G | — | uncertain significance |
| rs560304943 | 8:95,508,703 | G/C | — | uncertain significance |
| rs1813892539 | 8:95,511,604 | T/C | — | uncertain significance |
| rs149999621 | 8:95,511,660 | C/A | — | uncertain significance |
| rs4269508 | 8:95,512,399 | G/C | — | — |
| rs10956915 | 8:95,514,590 | C/T | intron variant | — |
| rs769100718 | 8:95,518,827 | G/A | — | uncertain significance |
| rs12678305 | 8:95,521,139 | T/C | intron variant | — |
| rs2488100693 | 8:95,521,948 | C/T | — | likely benign |
| rs775904242 | 8:95,521,981 | C/T | — | uncertain significance |
| rs768635531 | 8:95,521,992 | C/T | — | uncertain significance |
| rs770482412 | 8:95,522,059 | T/G | — | uncertain significance |
| rs199503113 | 8:95,522,700 | T/A | — | uncertain significance |
| rs949843788 | 8:95,522,750 | T/C | — | uncertain significance |
| rs1486402436 | 8:95,522,765 | G/A | — | uncertain significance |
| rs1814333970 | 8:95,522,873 | T/C | — | uncertain significance |
| rs2488107611 | 8:95,523,603 | A/G | — | uncertain significance |
| rs2488107771 | 8:95,523,646 | A/C | — | uncertain significance |
| rs770093691 | 8:95,524,250 | A/G | — | uncertain significance |
| rs755980531 | 8:95,530,083 | C/T | — | uncertain significance |
| rs144634788 | 8:95,530,099 | G/A | — | uncertain significance |
| rs1814616628 | 8:95,530,108 | A/G | — | uncertain significance |
| rs750430664 | 8:95,531,333 | T/C | — | uncertain significance |
| rs550047879 | 8:95,538,545 | G/T | — | uncertain significance |
| rs1057126526 | 8:95,538,616 | A/G | — | uncertain significance |
| rs902763170 | 8:95,538,736 | G/C | — | uncertain significance |
| rs1472040981 | 8:95,538,774 | A/C | — | uncertain significance |
| rs1814977330 | 8:95,538,789 | T/G | — | uncertain significance |
| rs571574560 | 8:95,538,793 | T/C | — | uncertain significance |
| rs1814977619 | 8:95,538,799 | T/C | — | uncertain significance |
| rs773832011 | 8:95,538,815 | T/C | — | uncertain significance |
| rs762417400 | 8:95,538,868 | A/G | — | uncertain significance |
| rs1243914422 | 8:95,538,899 | G/T | — | uncertain significance |
| rs2488156987 | 8:95,538,958 | T/C | — | uncertain significance |
| rs1476994906 | 8:95,539,022 | T/C | — | uncertain significance |
| rs113939516 | 8:95,539,192 | G/C | — | uncertain significance |
| rs1426237222 | 8:95,539,330 | G/T | — | uncertain significance |
| rs947078421 | 8:95,539,345 | G/A | — | uncertain significance |
| rs1815008107 | 8:95,539,582 | C/A | — | uncertain significance |
| rs957448 | 8:95,541,302 | A/G | synonymous variant | — |
| rs369847047 | 8:95,541,393 | T/C | — | uncertain significance |
| rs970233539 | 8:95,541,435 | C/T | — | uncertain significance |
| rs2488164987 | 8:95,541,536 | T/G | — | uncertain significance |
| rs370751977 | 8:95,541,544 | G/A | — | uncertain significance |
| rs199741865 | 8:95,541,561 | T/A | — | uncertain significance |
| rs2488170016 | 8:95,543,205 | G/A | — | uncertain significance |
| rs139231722 | 8:95,547,117 | G/A | — | uncertain significance |
| rs143155767 | 8:95,547,150 | T/C | — | uncertain significance |
| rs573994447 | 8:95,549,373 | T/G | — | uncertain significance |
| rs150645423 | 8:95,550,513 | C/T | — | uncertain significance |
| rs374086333 | 8:95,556,067 | T/C | — | likely benign |
| rs1331570184 | 8:95,556,068 | T/C | — | uncertain significance |
| rs2488203449 | 8:95,556,112 | C/T | — | uncertain significance |
| rs762933893 | 8:95,565,620 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.