LARS2
leucyl-tRNA synthetase 2, mitochondrial
Summary
This gene encodes a class 1 aminoacyl-tRNA synthetase, mitochondrial leucyl-tRNA synthetase. Each of the twenty aminoacyl-tRNA synthetases catalyzes the aminoacylation of a specific tRNA or tRNA isoaccepting family with the cognate amino acid. [provided by RefSeq, Jul 2008]
Known Variants445 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs28413188 | 3:45,430,151 | G/A | — | benign |
| rs1553625369 | 3:45,430,157 | C/G | — | likely benign |
| rs767039300 | 3:45,430,178 | C/A | — | likely benign |
| rs1553625371 | 3:45,430,182 | C/G | — | likely benign |
| rs9860885 | 3:45,430,245 | C/G | — | benign |
| rs967355397 | 3:45,432,975 | C/A | — | likely benign |
| rs75054661 | 3:45,433,126 | G/A | — | benign |
| rs78674974 | 3:45,433,267 | C/G | — | likely benign |
| rs114795216 | 3:45,435,682 | T/C | — | likely benign |
| rs704923 | 3:45,435,849 | A/T | — | benign |
| rs779418705 | 3:45,435,912 | C/T | — | likely benign |
| rs77377258 | 3:45,435,967 | T/C | — | benign |
| rs1308542565 | 3:45,436,004 | A/G | — | uncertain significance |
| rs752704499 | 3:45,436,034 | G/A | — | uncertain significance |
| rs779796862 | 3:45,436,043 | T/C | — | uncertain significance |
| rs1020076031 | 3:45,436,047 | C/T | — | likely benign |
| rs113559893 | 3:45,436,048 | G/A | — | uncertain significance |
| rs2125671988 | 3:45,436,070 | G/A | — | uncertain significance |
| rs143095137 | 3:45,436,080 | A/T | — | uncertain significance |
| rs777694670 | 3:45,436,090 | A/G | — | uncertain significance |
| rs200135115 | 3:45,436,093 | G/A | — | uncertain significance |
| rs141607519 | 3:45,436,102 | T/C | — | benign |
| rs199568924 | 3:45,436,125 | G/C | — | uncertain significance |
| rs2125672068 | 3:45,436,131 | G/A | — | pathogenic |
| rs1213550131 | 3:45,436,134 | G/A | — | pathogenic |
| rs1214818871 | 3:45,436,141 | C/T | — | pathogenic |
| rs532725261 | 3:45,436,160 | C/T | — | conflicting classifications of pathogenicity |
| rs754475523 | 3:45,436,164 | A/G | — | likely benign |
| rs780865850 | 3:45,436,165 | A/G | — | uncertain significance |
| rs1698014670 | 3:45,436,189 | C/T | — | likely benign |
| rs376300134 | 3:45,436,197 | T/G | — | likely benign |
| rs770781729 | 3:45,436,199 | C/T | — | likely benign |
| rs41289596 | 3:45,436,225 | A/G | — | likely benign |
| rs17637580 | 3:45,436,473 | G/A | — | benign |
| rs17637703 | 3:45,440,721 | A/G | intron variant | — |
| rs147090571 | 3:45,441,397 | T/G | — | likely benign |
| rs1057524188 | 3:45,441,718 | C/A | — | likely benign |
| rs75240042 | 3:45,441,725 | G/A | — | likely benign |
| rs568080843 | 3:45,441,728 | C/T | — | likely benign |
| rs200577813 | 3:45,441,730 | T/G | — | likely benign |
| rs374194205 | 3:45,441,741 | C/T | — | uncertain significance |
| rs114881088 | 3:45,441,757 | C/T | — | likely benign |
| rs140589843 | 3:45,441,758 | G/A | — | uncertain significance |
| rs2125675498 | 3:45,441,777 | A/T | — | uncertain significance |
| rs2528755898 | 3:45,441,778 | T/A | — | pathogenic |
| rs993142041 | 3:45,441,779 | C/T | — | uncertain significance |
| rs2528756045 | 3:45,441,802 | C/T | — | likely benign |
| rs757204777 | 3:45,441,810 | G/A | — | likely pathogenic |
| rs765128246 | 3:45,441,817 | C/T | — | likely benign |
| rs556672032 | 3:45,441,819 | C/T | — | uncertain significance |
| rs140105027 | 3:45,441,826 | C/T | — | likely benign |
| rs1698123763 | 3:45,441,828 | A/G | — | uncertain significance |
| rs756093994 | 3:45,441,833 | A/G | — | uncertain significance |
| rs138437422 | 3:45,441,840 | G/A | — | conflicting classifications of pathogenicity |
| rs746182533 | 3:45,441,846 | A/G | — | uncertain significance |
| rs2528756365 | 3:45,441,853 | G/C | — | not provided |
| rs1326685338 | 3:45,441,861 | T/C | — | uncertain significance |
| rs200681375 | 3:45,441,864 | A/G | — | likely benign |
| rs201821626 | 3:45,441,873 | C/T | — | likely benign |
| rs944920117 | 3:45,441,878 | G/A | — | likely benign |
| rs376129780 | 3:45,441,879 | C/T | — | likely benign |
| rs73830408 | 3:45,441,907 | C/T | — | benign |
| rs17576289 | 3:45,458,733 | A/G | — | benign |
| rs73070309 | 3:45,458,751 | C/T | — | benign |
| rs911830225 | 3:45,458,974 | G/A | — | uncertain significance |
| rs776171893 | 3:45,458,981 | A/T | — | pathogenic |
| rs1575240334 | 3:45,458,998 | G/A | — | likely pathogenic |
| rs769192897 | 3:45,459,003 | T/C | — | likely benign |
| rs141415249 | 3:45,459,024 | C/T | — | likely benign |
| rs1553628118 | 3:45,459,026 | C/T | — | uncertain significance |
| rs764326133 | 3:45,459,030 | C/A | — | likely benign |
| rs1559462145 | 3:45,459,031 | G/A | — | uncertain significance |
| rs1403808001 | 3:45,459,034 | A/G | — | uncertain significance |
| rs1698449994 | 3:45,459,038 | A/G | — | uncertain significance |
| rs757290932 | 3:45,459,045 | T/C | — | likely benign |
| rs536853368 | 3:45,459,050 | A/C | — | likely pathogenic |
| rs1339786996 | 3:45,459,051 | A/G | — | likely benign |
| rs899202461 | 3:45,459,054 | T/C | — | likely benign |
| rs768935434 | 3:45,459,078 | A/G | — | likely benign |
| rs2286907 | 3:45,459,287 | G/T | — | benign |
| rs854202 | 3:45,460,914 | T/C | — | benign |
| rs1295035278 | 3:45,461,145 | T/C | — | likely benign |
| rs765621362 | 3:45,461,159 | A/G | — | likely pathogenic |
| rs786205560 | 3:45,461,162 | A/C | missense variant | pathogenic |
| rs1048780344 | 3:45,461,177 | A/G | — | uncertain significance |
| rs752015037 | 3:45,461,183 | C/T | — | pathogenic |
| rs755313380 | 3:45,461,192 | C/T | — | uncertain significance |
| rs150185028 | 3:45,461,193 | G/A | — | uncertain significance |
| rs777455679 | 3:45,461,212 | C/T | — | conflicting classifications of pathogenicity |
| rs1181823409 | 3:45,461,216 | G/T | — | uncertain significance |
| rs1698486400 | 3:45,461,229 | A/C | — | likely benign |
| rs854203 | 3:45,461,359 | A/G | — | benign |
| rs17638301 | 3:45,461,483 | A/G | — | benign |
| rs9825041 | 3:45,475,993 | A/G | intron variant | — |
| rs952621 | 3:45,476,694 | G/A | regulatory region variant | — |
| rs368452663 | 3:45,488,162 | C/T | — | likely benign |
| rs756497084 | 3:45,488,379 | G/A | — | likely benign |
| rs2125704198 | 3:45,488,386 | A/G | — | uncertain significance |
| rs1322452155 | 3:45,488,395 | T/A | — | uncertain significance |
| rs2528895745 | 3:45,488,406 | T/A | — | uncertain significance |
Showing 100 of 445 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.