ClinVar Miner

List of variants in gene QARS1 reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 53
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005051.3(QARS1):c.1671G>T (p.Val557=) rs115671018 0.00334
NM_005051.3(QARS1):c.877-17T>C rs374002070 0.00108
NM_005051.3(QARS1):c.1295+20G>C rs377586991 0.00048
NM_005051.3(QARS1):c.632-20C>T rs367637023 0.00029
NM_005051.3(QARS1):c.1388+7G>A rs201234869 0.00023
NM_005051.3(QARS1):c.1527-18C>T rs374752377 0.00021
NM_005051.3(QARS1):c.451+19G>A rs369141824 0.00021
NM_005051.3(QARS1):c.1758+17_1758+18del rs372006503 0.00015
NM_005051.3(QARS1):c.1864-15A>G rs374530633 0.00015
NM_005051.3(QARS1):c.877-15G>A rs368949211 0.00015
NM_005051.3(QARS1):c.118-5C>T rs778689182 0.00011
NM_005051.3(QARS1):c.703+17A>T rs60002662 0.00009
NM_005051.3(QARS1):c.1863+18A>C rs375666402 0.00007
NM_005051.3(QARS1):c.451+18C>T rs202145473 0.00007
NM_005051.3(QARS1):c.-21T>C rs372058541 0.00006
NM_005051.3(QARS1):c.-20T>C rs368345855 0.00005
NM_005051.3(QARS1):c.1122C>T (p.Pro374=) rs572025824 0.00004
NM_005051.3(QARS1):c.495C>T (p.Ile165=) rs375725197 0.00003
NM_005051.3(QARS1):c.693C>T (p.Phe231=) rs760938297 0.00003
NM_005051.3(QARS1):c.780T>C (p.Thr260=) rs367793549 0.00003
NM_005051.3(QARS1):c.9T>C (p.Ala3=) rs776233744 0.00002
NM_005051.3(QARS1):c.1056-13C>T rs369771745 0.00001
NM_005051.3(QARS1):c.1398C>G (p.Ser466=) rs370978363 0.00001
NM_005051.3(QARS1):c.1650A>G (p.Pro550=) rs762120492 0.00001
NM_005051.3(QARS1):c.1863+14G>A rs1057521351 0.00001
NM_005051.3(QARS1):c.1923A>G (p.Thr641=) rs764054134 0.00001
NM_005051.3(QARS1):c.1957-14C>T rs751375938 0.00001
NM_005051.3(QARS1):c.2151+11G>T rs774818694 0.00001
NM_005051.3(QARS1):c.2151+13G>C rs1465310490 0.00001
NM_005051.3(QARS1):c.266-15G>A rs761737038 0.00001
NM_005051.3(QARS1):c.266-17G>A rs1057523447 0.00001
NM_005051.3(QARS1):c.295T>C (p.Leu99=) rs754138545 0.00001
NM_005051.3(QARS1):c.452-10A>G rs754207465 0.00001
NM_005051.3(QARS1):c.516+13C>A rs754227489 0.00001
NM_005051.3(QARS1):c.570+16G>T rs1479784080 0.00001
NM_005051.3(QARS1):c.687T>G (p.Leu229=) rs1479459378 0.00001
NM_005051.3(QARS1):c.789+3G>A rs536602071 0.00001
NM_005051.3(QARS1):c.960C>T (p.Asp320=) rs780978358 0.00001
NM_005051.2(QARS1):c.-32C>A rs376348627
NM_005051.3(QARS1):c.1388+17C>T rs1553751829
NM_005051.3(QARS1):c.1526+13G>C rs775939776
NM_005051.3(QARS1):c.1759-13_1759-7del rs781635166
NM_005051.3(QARS1):c.1863+10G>C rs749903302
NM_005051.3(QARS1):c.1863+14G>T rs1057521351
NM_005051.3(QARS1):c.1957-22_1957-20del rs753102798
NM_005051.3(QARS1):c.2152-9T>C rs1057524221
NM_005051.3(QARS1):c.2304G>A (p.Leu768=) rs767099836
NM_005051.3(QARS1):c.243C>T (p.Ile81=) rs754974684
NM_005051.3(QARS1):c.549T>C (p.Ala183=) rs150572774
NM_005051.3(QARS1):c.571-17C>T rs773560133
NM_005051.3(QARS1):c.632-10dup rs775642346
NM_005051.3(QARS1):c.632-13T>C rs532499007
NM_005051.3(QARS1):c.837A>T (p.Gly279=) rs1057523072

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.