EEF2KMT
eukaryotic elongation factor 2 lysine methyltransferase
Summary
Enables protein-lysine N-methyltransferase activity. Involved in peptidyl-lysine trimethylation. Located in cytoplasm. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1957081691 | 16:5,134,559 | G/A | — | benign |
| rs776562609 | 16:5,135,646 | T/G | — | uncertain significance |
| rs201345819 | 16:5,135,659 | T/C | — | uncertain significance |
| rs772676442 | 16:5,135,730 | C/T | — | likely benign |
| rs36073823 | 16:5,138,259 | T/C | — | — |
| rs140633124 | 16:5,139,114 | C/T | — | uncertain significance |
| rs377526564 | 16:5,139,150 | C/T | — | likely benign |
| rs776203089 | 16:5,139,183 | G/T | — | uncertain significance |
| rs766915913 | 16:5,139,189 | C/G | — | uncertain significance |
| rs149513493 | 16:5,139,191 | C/T | — | likely benign |
| rs3204207 | 16:5,139,192 | G/A | — | uncertain significance |
| rs757034789 | 16:5,139,203 | A/G | — | uncertain significance |
| rs201731046 | 16:5,139,209 | C/T | — | likely benign |
| rs780858727 | 16:5,139,219 | C/T | — | uncertain significance |
| rs137885504 | 16:5,139,230 | A/T | — | uncertain significance |
| rs570051680 | 16:5,139,255 | C/T | — | uncertain significance |
| rs866690231 | 16:5,140,115 | C/T | — | uncertain significance |
| rs149687558 | 16:5,140,135 | G/A | — | likely benign |
| rs755592437 | 16:5,140,178 | C/G | — | uncertain significance |
| rs771934768 | 16:5,140,189 | G/A | — | uncertain significance |
| rs750093237 | 16:5,140,214 | C/T | — | uncertain significance |
| rs746870637 | 16:5,140,256 | T/C | — | uncertain significance |
| rs200554884 | 16:5,140,282 | C/T | — | uncertain significance |
| rs377613734 | 16:5,140,289 | G/A | — | uncertain significance |
| rs140512475 | 16:5,140,324 | G/A | — | likely benign |
| rs768403270 | 16:5,140,506 | C/T | — | uncertain significance |
| rs573199881 | 16:5,140,515 | C/T | — | uncertain significance |
| rs542077714 | 16:5,140,553 | G/A | — | uncertain significance |
| rs375999506 | 16:5,140,556 | C/T | — | likely benign |
| rs556347926 | 16:5,141,808 | C/T | — | uncertain significance |
| rs147889190 | 16:5,141,847 | G/A | — | uncertain significance |
| rs138387891 | 16:5,143,534 | G/T | — | uncertain significance |
| rs775889559 | 16:5,143,552 | G/A | — | uncertain significance |
| rs753962687 | 16:5,143,565 | T/A | — | uncertain significance |
| rs1298821277 | 16:5,145,458 | G/A | — | uncertain significance |
| rs147997807 | 16:5,145,473 | G/C | — | uncertain significance |
| rs1251608202 | 16:5,147,652 | G/T | — | uncertain significance |
| rs967716619 | 16:5,147,653 | G/A | — | uncertain significance |
| rs760291464 | 16:5,147,671 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.