METTL13
methyltransferase 13, eEF1A N-terminus and K55
Summary
Enables protein-lysine N-methyltransferase activity. Predicted to be involved in methylation. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs368751643 | 1:171,751,190 | C/A | — | uncertain significance |
| rs1553264586 | 1:171,751,202 | A/G | — | uncertain significance |
| rs2294720 | 1:171,751,236 | T/C | — | benign |
| rs763335545 | 1:171,752,958 | G/A | — | uncertain significance |
| rs749884051 | 1:171,752,979 | A/G | — | uncertain significance |
| rs2528107533 | 1:171,753,013 | C/A | — | uncertain significance |
| rs2232816 | 1:171,753,039 | A/G | — | benign |
| rs1402209615 | 1:171,753,085 | A/G | — | uncertain significance |
| rs765001555 | 1:171,753,098 | G/C | — | likely benign |
| rs1656912722 | 1:171,753,129 | A/T | — | uncertain significance |
| rs371404027 | 1:171,753,163 | T/C | — | uncertain significance |
| rs373455201 | 1:171,753,189 | C/T | — | uncertain significance |
| rs2528108276 | 1:171,753,229 | A/G | — | uncertain significance |
| rs768804578 | 1:171,753,257 | G/T | — | uncertain significance |
| rs141898298 | 1:171,753,275 | G/A | — | benign |
| rs2528108721 | 1:171,753,306 | T/A | — | uncertain significance |
| rs773923048 | 1:171,753,381 | G/T | — | uncertain significance |
| rs149021718 | 1:171,753,386 | T/A | — | likely benign |
| rs778251374 | 1:171,753,426 | G/A | — | uncertain significance |
| rs764468762 | 1:171,753,461 | G/A | — | likely benign |
| rs746708716 | 1:171,753,507 | C/T | — | uncertain significance |
| rs200794655 | 1:171,753,508 | G/A | — | uncertain significance |
| rs780483296 | 1:171,753,554 | C/A | — | uncertain significance |
| rs754351572 | 1:171,753,556 | C/T | — | uncertain significance |
| rs61733149 | 1:171,753,613 | G/A | — | benign |
| rs756717714 | 1:171,755,031 | G/A | — | uncertain significance |
| rs146649028 | 1:171,755,041 | G/A | — | likely benign |
| rs1656992296 | 1:171,755,057 | G/A | — | uncertain significance |
| rs17650204 | 1:171,755,071 | G/A | — | benign |
| rs2528115374 | 1:171,755,085 | G/A | — | uncertain significance |
| rs2232818 | 1:171,755,170 | G/A | — | benign |
| rs201618453 | 1:171,755,180 | A/T | — | uncertain significance |
| rs2232819 | 1:171,755,182 | G/A | — | benign |
| rs1465300285 | 1:171,755,186 | C/G | — | uncertain significance |
| rs149501332 | 1:171,755,199 | G/C | — | uncertain significance |
| rs1657067685 | 1:171,756,901 | C/G | — | uncertain significance |
| rs148254472 | 1:171,756,916 | C/A | — | likely benign |
| rs201682767 | 1:171,756,954 | A/G | — | uncertain significance |
| rs2232821 | 1:171,757,036 | C/T | — | benign |
| rs776191727 | 1:171,757,069 | A/C | — | uncertain significance |
| rs34320898 | 1:171,759,139 | G/C | intron variant | — |
| rs541143010 | 1:171,759,631 | C/A | — | uncertain significance |
| rs144305462 | 1:171,759,661 | C/T | — | uncertain significance |
| rs748855096 | 1:171,759,673 | T/C | — | uncertain significance |
| rs200895209 | 1:171,759,765 | G/C | — | likely benign |
| rs2232822 | 1:171,761,191 | C/T | — | benign |
| rs1558132684 | 1:171,761,192 | G/A | — | uncertain significance |
| rs752310306 | 1:171,761,207 | C/G | — | uncertain significance |
| rs371883088 | 1:171,761,240 | A/C | — | uncertain significance |
| rs762043608 | 1:171,761,258 | G/T | — | uncertain significance |
| rs375223887 | 1:171,761,264 | T/C | — | uncertain significance |
| rs145666727 | 1:171,761,313 | G/A | — | risk factor |
| rs990538098 | 1:171,761,327 | A/G | — | uncertain significance |
| rs772705665 | 1:171,761,351 | G/T | — | uncertain significance |
| rs1657232794 | 1:171,761,367 | G/A | — | uncertain significance |
| rs138325418 | 1:171,763,538 | C/T | — | uncertain significance |
| rs2232825 | 1:171,763,549 | T/C | — | benign |
| rs201545508 | 1:171,763,595 | A/C | — | benign |
| rs61733150 | 1:171,763,627 | A/G | — | benign |
| rs371081946 | 1:171,763,640 | A/G | — | uncertain significance |
| rs200909388 | 1:171,763,662 | C/A | — | uncertain significance |
| rs369407003 | 1:171,765,649 | G/A | — | uncertain significance |
| rs368473341 | 1:171,765,691 | C/A | — | uncertain significance |
| rs371747669 | 1:171,765,714 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.