EEFSEC
eukaryotic elongation factor, selenocysteine-tRNA specific
Summary
Enables GTPase activity. Involved in selenocysteine incorporation. Predicted to be located in cytoplasm and nucleus. Predicted to be part of ribonucleoprotein complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants68 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs567446865 | 3:127,872,405 | G/A | — | uncertain significance |
| rs1164834792 | 3:127,872,464 | G/T | — | uncertain significance |
| rs934315994 | 3:127,872,480 | G/C | — | uncertain significance |
| rs756976693 | 3:127,872,483 | C/G | — | uncertain significance |
| rs148745324 | 3:127,872,494 | G/T | — | likely benign |
| rs565711771 | 3:127,872,526 | C/A | — | uncertain significance |
| rs1003961919 | 3:127,872,537 | C/T | — | uncertain significance |
| rs751970437 | 3:127,872,594 | G/A | — | uncertain significance |
| rs2999052 | 3:127,892,037 | T/C | intron variant | — |
| rs2687729 | 3:127,895,226 | A/G | intron variant | — |
| rs2999089 | 3:127,935,159 | C/A | — | — |
| rs2955133 | 3:127,945,322 | T/C | intron variant | — |
| rs6809833 | 3:127,952,919 | A/C | — | — |
| rs56397996 | 3:127,954,710 | T/C | — | — |
| rs2955083 | 3:127,961,178 | T/A | intron variant | — |
| rs2473595635 | 3:127,965,792 | G/T | — | uncertain significance |
| rs2066135206 | 3:127,965,804 | A/G | — | uncertain significance |
| rs181759924 | 3:127,965,816 | C/T | — | uncertain significance |
| rs775158694 | 3:127,965,850 | T/G | — | uncertain significance |
| rs1371128960 | 3:127,965,867 | A/G | — | uncertain significance |
| rs1378138401 | 3:127,980,976 | G/A | — | uncertain significance |
| rs369240402 | 3:127,980,985 | C/T | — | uncertain significance |
| rs116353475 | 3:127,980,986 | G/A | — | benign |
| rs373534963 | 3:127,980,996 | G/T | — | uncertain significance |
| rs763279916 | 3:127,981,062 | A/G | — | uncertain significance |
| rs568685973 | 3:127,981,063 | T/C | — | uncertain significance |
| rs773260814 | 3:127,983,530 | G/A | — | uncertain significance |
| rs759747927 | 3:127,983,577 | T/A | — | uncertain significance |
| rs2811373 | 3:127,997,429 | T/A | intron variant | — |
| rs2811525 | 3:127,999,430 | T/A | — | — |
| rs56287882 | 3:128,030,343 | G/A | intron variant | — |
| rs115119067 | 3:128,031,871 | G/A | intron variant | — |
| rs10934853 | 3:128,038,373 | C/G | — | — |
| rs12486127 | 3:128,038,689 | C/A | intron variant | — |
| rs56328893 | 3:128,041,830 | A/G | intron variant | — |
| rs750034735 | 3:128,060,100 | C/A | — | uncertain significance |
| rs140543627 | 3:128,060,143 | G/A | — | uncertain significance |
| rs773008456 | 3:128,060,190 | G/A | — | uncertain significance |
| rs199722086 | 3:128,060,208 | G/A | — | uncertain significance |
| rs146372467 | 3:128,060,254 | T/C | — | uncertain significance |
| rs749490556 | 3:128,060,257 | C/T | — | uncertain significance |
| rs1171115208 | 3:128,060,458 | A/C | — | likely pathogenic |
| rs779804328 | 3:128,060,502 | C/T | — | uncertain significance |
| rs34326479 | 3:128,060,593 | C/T | — | benign |
| rs776954210 | 3:128,060,617 | G/A | — | uncertain significance |
| rs775849626 | 3:128,060,640 | C/T | — | uncertain significance |
| rs112227741 | 3:128,060,678 | C/G | — | uncertain significance |
| rs61044849 | 3:128,065,466 | C/T | intron variant | — |
| rs771158258 | 3:128,077,087 | C/T | — | uncertain significance |
| rs2472702137 | 3:128,077,093 | C/G | — | uncertain significance |
| rs2472702407 | 3:128,077,118 | A/T | — | uncertain significance |
| rs117458735 | 3:128,077,126 | G/A | — | uncertain significance |
| rs779354673 | 3:128,077,159 | C/A | — | uncertain significance |
| rs769768061 | 3:128,077,183 | G/A | — | uncertain significance |
| rs149272765 | 3:128,104,469 | C/T | regulatory region variant | — |
| rs561894280 | 3:128,108,611 | C/G | — | — |
| rs1702136 | 3:128,118,711 | G/C | — | — |
| rs972075769 | 3:128,126,958 | G/T | — | uncertain significance |
| rs376674260 | 3:128,126,969 | G/A | — | uncertain significance |
| rs200217143 | 3:128,126,978 | G/T | — | uncertain significance |
| rs755485270 | 3:128,127,010 | G/A | — | uncertain significance |
| rs373807553 | 3:128,127,014 | G/A | — | uncertain significance |
| rs568481175 | 3:128,127,050 | C/T | — | uncertain significance |
| rs114096655 | 3:128,127,053 | T/G | — | benign |
| rs372392092 | 3:128,127,059 | G/C | — | uncertain significance |
| rs558222018 | 3:128,127,082 | C/T | — | uncertain significance |
| rs116329335 | 3:128,127,083 | G/A | — | benign |
| rs142819202 | 3:128,127,086 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.