ClinVar Miner

List of variants in gene QARS1 reported as uncertain significance by GeneDx

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Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_005051.3(QARS1):c.2123C>T (p.Pro708Leu) rs142327602 0.00108
NM_005051.3(QARS1):c.1760C>T (p.Ser587Phe) rs144563810 0.00061
NM_005051.3(QARS1):c.1051C>T (p.Arg351Cys) rs763901654 0.00037
NM_005051.3(QARS1):c.316G>A (p.Asp106Asn) rs141983717 0.00034
NM_005051.3(QARS1):c.2261A>G (p.Asp754Gly) rs142480574 0.00026
NM_005051.3(QARS1):c.1246G>A (p.Val416Ile) rs147076980 0.00024
NM_005051.3(QARS1):c.451+4A>C rs370688039 0.00022
NM_005051.3(QARS1):c.1568G>A (p.Arg523Gln) rs201013732 0.00021
NM_005051.3(QARS1):c.400C>T (p.Arg134Trp) rs142831772 0.00018
NM_005051.3(QARS1):c.143T>C (p.Ile48Thr) rs201397059 0.00016
NM_005051.3(QARS1):c.1195G>A (p.Glu399Lys) rs143072084 0.00014
NM_005051.3(QARS1):c.1712T>C (p.Val571Ala) rs755259427 0.00014
NM_005051.3(QARS1):c.337G>A (p.Val113Met) rs767616063 0.00011
NM_005051.3(QARS1):c.461G>A (p.Arg154Gln) rs201032950 0.00010
NM_005051.3(QARS1):c.1585C>T (p.Pro529Ser) rs373719958 0.00009
NM_005051.3(QARS1):c.1559C>T (p.Thr520Met) rs764216449 0.00006
NM_005051.3(QARS1):c.1759-13T>A rs375454834 0.00006
NM_005051.3(QARS1):c.2210C>T (p.Pro737Leu) rs772699618 0.00006
NM_005051.3(QARS1):c.297G>C (p.Leu99Phe) rs147794116 0.00006
NM_005051.3(QARS1):c.601C>T (p.Arg201Trp) rs200703354 0.00006
NM_005051.3(QARS1):c.1158C>T (p.Leu386=) rs1085307775 0.00005
NM_005051.3(QARS1):c.1613G>A (p.Arg538Gln) rs778807845 0.00005
NM_005051.3(QARS1):c.1304A>G (p.Tyr435Cys) rs143462532 0.00004
NM_005051.3(QARS1):c.2215G>A (p.Asp739Asn) rs749055007 0.00004
NM_005051.3(QARS1):c.697A>C (p.Lys233Gln) rs1248234116 0.00004
NM_005051.3(QARS1):c.1085G>T (p.Gly362Val) rs763512186 0.00003
NM_005051.3(QARS1):c.1284_1285del (p.Asp430fs) rs775652214 0.00003
NM_005051.3(QARS1):c.1292A>C (p.Lys431Thr) rs778340693 0.00003
NM_005051.3(QARS1):c.2069G>A (p.Arg690His) rs201781920 0.00003
NM_005051.3(QARS1):c.901C>T (p.Arg301Cys) rs1370265763 0.00003
NM_005051.3(QARS1):c.1189G>C (p.Glu397Gln) rs758759632 0.00002
NM_005051.3(QARS1):c.1255C>T (p.Arg419Ter) rs769378726 0.00002
NM_005051.3(QARS1):c.1614+3A>G rs1485211824 0.00002
NM_005051.3(QARS1):c.2075A>G (p.Tyr692Cys) rs557972227 0.00002
NM_005051.3(QARS1):c.262A>C (p.Ser88Arg) rs751342771 0.00002
NM_005051.3(QARS1):c.602G>A (p.Arg201Gln) rs192040640 0.00002
NM_005051.3(QARS1):c.1060C>G (p.Leu354Val) rs1370961350 0.00001
NM_005051.3(QARS1):c.1170G>A (p.Met390Ile) rs1559967769 0.00001
NM_005051.3(QARS1):c.1231G>A (p.Gly411Ser) rs765950058 0.00001
NM_005051.3(QARS1):c.1280G>A (p.Arg427His) rs148004466 0.00001
NM_005051.3(QARS1):c.128C>G (p.Thr43Ser) rs550717519 0.00001
NM_005051.3(QARS1):c.1315G>A (p.Asp439Asn) rs764347049 0.00001
NM_005051.3(QARS1):c.1774G>C (p.Val592Leu) rs751191501 0.00001
NM_005051.3(QARS1):c.2234G>A (p.Arg745His) rs770019480 0.00001
NM_005051.3(QARS1):c.2317G>A (p.Gly773Arg) rs762570876 0.00001
NM_005051.3(QARS1):c.419A>G (p.Glu140Gly) rs750778308 0.00001
NM_005051.3(QARS1):c.557A>G (p.Glu186Gly) rs1346246672 0.00001
NM_005051.3(QARS1):c.1199C>T (p.Ala400Val) rs1386524025
NM_005051.3(QARS1):c.1418C>T (p.Ala473Val) rs1064797070
NM_005051.3(QARS1):c.1468C>T (p.His490Tyr)
NM_005051.3(QARS1):c.149A>G (p.Lys50Arg) rs1559970922
NM_005051.3(QARS1):c.151G>C (p.Ala51Pro) rs755697141
NM_005051.3(QARS1):c.1527-6C>G rs1454109423
NM_005051.3(QARS1):c.1664C>G (p.Ala555Gly)
NM_005051.3(QARS1):c.1739_1741del (p.Thr580del)
NM_005051.3(QARS1):c.1746T>G (p.Phe582Leu)
NM_005051.3(QARS1):c.1756A>C (p.Lys586Gln) rs2107098757
NM_005051.3(QARS1):c.1832T>C (p.Ile611Thr) rs757743183
NM_005051.3(QARS1):c.250delinsAAGA (p.Glu84delinsLysLys) rs2107113849
NM_005051.3(QARS1):c.346A>G (p.Ile116Val)
NM_005051.3(QARS1):c.799C>T (p.Arg267Trp)
NM_005051.3(QARS1):c.851T>G (p.Ile284Ser)
NM_005051.3(QARS1):c.858C>A (p.Phe286Leu) rs1307590384
NM_005051.3(QARS1):c.869A>G (p.Tyr290Cys)
NM_005051.3(QARS1):c.884A>C (p.Asn295Thr) rs540036773
NM_005051.3(QARS1):c.895T>C (p.Phe299Leu)
NM_005051.3(QARS1):c.988T>A (p.Tyr330Asn) rs2107103622

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