LENG8
leukocyte receptor cluster member 8
Summary
Predicted to be part of protein-containing complex. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs189073512 | 19:54,960,020 | T/C | coding sequence variant | — |
| rs765124532 | 19:54,962,547 | G/A | — | uncertain significance |
| rs769292827 | 19:54,963,323 | C/T | — | uncertain significance |
| rs111838811 | 19:54,963,333 | C/T | — | likely benign |
| rs758737426 | 19:54,963,400 | G/A | — | likely benign |
| rs373837656 | 19:54,963,422 | A/G | — | uncertain significance |
| rs2514481224 | 19:54,963,425 | G/T | — | uncertain significance |
| rs763227520 | 19:54,963,840 | A/G | — | uncertain significance |
| rs146623714 | 19:54,963,871 | G/C | — | benign |
| rs528046612 | 19:54,964,524 | C/T | — | — |
| rs781125144 | 19:54,964,729 | T/C | — | uncertain significance |
| rs201939037 | 19:54,964,806 | G/A | — | uncertain significance |
| rs964005888 | 19:54,965,621 | G/A | — | uncertain significance |
| rs2514515112 | 19:54,965,649 | C/T | — | uncertain significance |
| rs1481881330 | 19:54,965,694 | A/T | — | uncertain significance |
| rs148099604 | 19:54,965,739 | G/C | — | uncertain significance |
| rs751624153 | 19:54,965,741 | A/C | — | uncertain significance |
| rs368445549 | 19:54,965,776 | C/T | — | likely benign |
| rs141841613 | 19:54,965,777 | G/A | — | uncertain significance |
| rs1053132543 | 19:54,965,817 | C/G | — | uncertain significance |
| rs544936953 | 19:54,965,825 | C/T | — | uncertain significance |
| rs200747306 | 19:54,966,148 | G/A | — | uncertain significance |
| rs147412771 | 19:54,966,175 | C/A | — | uncertain significance |
| rs747883265 | 19:54,966,187 | C/A | — | uncertain significance |
| rs141287435 | 19:54,966,694 | C/T | — | likely benign |
| rs763487701 | 19:54,966,728 | G/A | — | uncertain significance |
| rs138334094 | 19:54,966,744 | G/A | — | likely benign |
| rs1042348119 | 19:54,967,185 | G/T | — | uncertain significance |
| rs769571380 | 19:54,967,186 | C/T | — | uncertain significance |
| rs1393689738 | 19:54,967,194 | G/T | — | uncertain significance |
| rs745505732 | 19:54,967,226 | C/T | — | uncertain significance |
| rs772315116 | 19:54,967,295 | G/A | — | uncertain significance |
| rs2514556036 | 19:54,967,341 | C/G | — | uncertain significance |
| rs2514556612 | 19:54,967,357 | T/C | — | uncertain significance |
| rs748236940 | 19:54,967,379 | G/A | — | uncertain significance |
| rs75472495 | 19:54,967,408 | C/T | — | benign |
| rs147401836 | 19:54,967,577 | C/G | — | uncertain significance |
| rs750373164 | 19:54,967,586 | C/T | — | uncertain significance |
| rs756247660 | 19:54,967,591 | C/T | — | likely benign |
| rs778199336 | 19:54,967,629 | C/T | — | uncertain significance |
| rs377636837 | 19:54,967,827 | G/A | — | likely benign |
| rs1413424585 | 19:54,967,883 | G/A | — | uncertain significance |
| rs775233160 | 19:54,967,934 | G/A | — | uncertain significance |
| rs2514578551 | 19:54,968,030 | G/T | — | uncertain significance |
| rs35336528 | 19:54,968,038 | A/G | — | benign |
| rs149847702 | 19:54,968,314 | C/T | downstream gene variant | — |
| rs79857932 | 19:54,968,917 | C/T | — | benign |
| rs146190817 | 19:54,968,946 | C/G | — | uncertain significance |
| rs780417567 | 19:54,968,985 | G/A | — | likely benign |
| rs551413817 | 19:54,969,127 | C/T | — | likely benign |
| rs79561966 | 19:54,969,169 | C/T | — | benign |
| rs375131539 | 19:54,969,314 | G/A | — | likely benign |
| rs368155889 | 19:54,969,333 | G/A | — | uncertain significance |
| rs1293191015 | 19:54,969,513 | T/A | — | uncertain significance |
| rs2514607041 | 19:54,969,586 | G/A | — | uncertain significance |
| rs772620980 | 19:54,969,624 | C/T | — | uncertain significance |
| rs766932229 | 19:54,969,640 | A/G | — | uncertain significance |
| rs144060557 | 19:54,969,675 | G/C | — | uncertain significance |
| rs539586692 | 19:54,971,955 | T/A | — | likely benign |
| rs555749514 | 19:54,972,014 | G/A | — | uncertain significance |
| rs374952695 | 19:54,972,053 | C/T | — | uncertain significance |
| rs1471235144 | 19:54,972,092 | A/G | — | uncertain significance |
| rs117449644 | 19:54,972,163 | C/T | downstream gene variant | — |
| rs151232371 | 19:54,972,546 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.