ClinVar Miner

List of variants in gene AARS2 reported as uncertain significance by GeneDx

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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_020745.4(AARS2):c.1162C>T (p.Pro388Ser) rs139372744 0.00197
NM_020745.4(AARS2):c.2905G>T (p.Asp969Tyr) rs150039184 0.00123
NM_020745.4(AARS2):c.1534G>C (p.Asp512His) rs146512155 0.00073
NM_020745.4(AARS2):c.1195A>C (p.Asn399His) rs148363748 0.00059
NM_020745.4(AARS2):c.1660C>T (p.Arg554Cys) rs146924860 0.00058
NM_020745.4(AARS2):c.2630G>A (p.Arg877Gln) rs141941157 0.00048
NM_020745.4(AARS2):c.1645G>A (p.Val549Met) rs140408107 0.00025
NM_020745.4(AARS2):c.1157C>T (p.Ala386Val) rs143271585 0.00017
NM_020745.4(AARS2):c.1756G>A (p.Val586Met) rs201873561 0.00016
NM_020745.4(AARS2):c.2471T>C (p.Ile824Thr) rs146765163 0.00016
NM_020745.4(AARS2):c.2551C>G (p.Leu851Val) rs376103315 0.00014
NM_020745.4(AARS2):c.785G>A (p.Arg262Gln) rs139974034 0.00014
NM_020745.4(AARS2):c.1076G>A (p.Arg359His) rs200485499 0.00011
NM_020745.4(AARS2):c.422G>A (p.Gly141Asp) rs373555804 0.00009
NM_020745.4(AARS2):c.673C>T (p.His225Tyr) rs200704447 0.00009
NM_020745.4(AARS2):c.1067G>A (p.Arg356Gln) rs138470959 0.00008
NM_020745.4(AARS2):c.761G>C (p.Gly254Ala) rs199919912 0.00007
NM_020745.4(AARS2):c.10T>A (p.Ser4Thr) rs755011099 0.00006
NM_020745.4(AARS2):c.407A>G (p.Asn136Ser) rs781255698 0.00006
NM_020745.4(AARS2):c.2297T>G (p.Ile766Ser) rs200410313 0.00004
NM_020745.4(AARS2):c.2329C>T (p.Arg777Cys) rs568086131 0.00004
NM_020745.4(AARS2):c.2893G>A (p.Gly965Arg) rs543267101 0.00004
NM_020745.4(AARS2):c.2861C>T (p.Ala954Val) rs747312867 0.00003
NM_020745.4(AARS2):c.572T>G (p.Leu191Arg) rs757341602 0.00003
NM_020745.4(AARS2):c.1570G>A (p.Gly524Arg) rs772600706 0.00002
NM_020745.4(AARS2):c.2812A>C (p.Thr938Pro) rs763868546 0.00002
NM_020745.4(AARS2):c.670A>C (p.Ile224Leu) rs772630843 0.00002
NM_020745.4(AARS2):c.1366A>G (p.Met456Val) rs370375429 0.00001
NM_020745.4(AARS2):c.1445G>A (p.Arg482Gln) rs368303351 0.00001
NM_020745.4(AARS2):c.1486G>A (p.Val496Ile) rs1302029500 0.00001
NM_020745.4(AARS2):c.1519G>C (p.Val507Leu) rs182596701 0.00001
NM_020745.4(AARS2):c.1565C>G (p.Pro522Arg) rs908356412 0.00001
NM_020745.4(AARS2):c.1696G>A (p.Ala566Thr) rs764610166 0.00001
NM_020745.4(AARS2):c.1739G>A (p.Arg580Gln) rs749217850 0.00001
NM_020745.4(AARS2):c.2032C>T (p.Arg678Trp) rs751523537 0.00001
NM_020745.4(AARS2):c.2050G>C (p.Val684Leu) rs979593679 0.00001
NM_020745.4(AARS2):c.2207C>T (p.Pro736Leu) rs863223861 0.00001
NM_020745.4(AARS2):c.2210C>G (p.Ala737Gly) rs1362064811 0.00001
NM_020745.4(AARS2):c.325G>T (p.Val109Leu) rs747882284 0.00001
NM_020745.4(AARS2):c.946C>T (p.Arg316Cys) rs765720580 0.00001
NM_020745.4(AARS2):c.1089G>C (p.Glu363Asp)
NM_020745.4(AARS2):c.1145C>T (p.Thr382Ile)
NM_020745.4(AARS2):c.1199T>C (p.Leu400Pro) rs2534681703
NM_020745.4(AARS2):c.1612C>A (p.Leu538Met) rs527544325
NM_020745.4(AARS2):c.1669C>T (p.Leu557Phe)
NM_020745.4(AARS2):c.1699G>A (p.Glu567Lys) rs763561398
NM_020745.4(AARS2):c.2305C>T (p.Arg769Cys) rs140918846
NM_020745.4(AARS2):c.2330G>A (p.Arg777His)
NM_020745.4(AARS2):c.2528A>G (p.Glu843Gly)
NM_020745.4(AARS2):c.2542G>A (p.Val848Met) rs2153353779
NM_020745.4(AARS2):c.25G>A (p.Ala9Thr) rs537231845
NM_020745.4(AARS2):c.25G>T (p.Ala9Ser) rs537231845
NM_020745.4(AARS2):c.2701C>T (p.Arg901Trp) rs145086947
NM_020745.4(AARS2):c.2722C>A (p.Pro908Thr)
NM_020745.4(AARS2):c.2722C>T (p.Pro908Ser) rs202149382
NM_020745.4(AARS2):c.31_39del (p.Leu12_Arg14del) rs562829310
NM_020745.4(AARS2):c.401T>C (p.Leu134Pro)
NM_020745.4(AARS2):c.424G>A (p.Glu142Lys) rs1554149186
NM_020745.4(AARS2):c.539T>C (p.Leu180Pro) rs2153357304
NM_020745.4(AARS2):c.566T>G (p.Ile189Ser)
NM_020745.4(AARS2):c.653G>C (p.Cys218Ser)
NM_020745.4(AARS2):c.755C>G (p.Ala252Gly) rs748309472
NM_020745.4(AARS2):c.816G>T (p.Arg272Ser) rs2534712602

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