ClinVar Miner

List of variants in gene TARS2 reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP gnomAD frequency
NM_025150.5(TARS2):c.696-284A>G rs7549396 0.75570
NM_025150.5(TARS2):c.67-166A>G rs2275246 0.61711
NM_025150.5(TARS2):c.388-266C>T rs9436118 0.59040
NM_025150.5(TARS2):c.1238+256T>G rs11576422 0.31055
NM_025150.5(TARS2):c.1238+99C>A rs11590324 0.30924
NM_025150.5(TARS2):c.1238+255C>A rs11590353 0.30898
NM_025150.5(TARS2):c.1719-47C>T rs3738487 0.29599
NM_025150.5(TARS2):c.1618-295G>A rs11205385 0.29567
NM_025150.5(TARS2):c.512+325T>C rs12145082 0.26402
NM_025150.5(TARS2):c.775-116A>G rs1343965 0.23233
NM_025150.5(TARS2):c.513-98C>G rs7542068 0.23142
NM_025150.5(TARS2):c.1238+73G>A rs11588874 0.23103
NM_025150.4(TARS2):c.-212T>C rs34001546 0.12563
NM_025150.5(TARS2):c.1020+96C>T rs12119249 0.11137
NM_025150.5(TARS2):c.695+193C>G rs112103825 0.08370
NM_025150.5(TARS2):c.387+238A>G rs12142874 0.08365
NM_025150.5(TARS2):c.387+310G>T rs12138453 0.08365
NM_025150.5(TARS2):c.1401+16C>T rs34542152 0.06320
NM_025150.5(TARS2):c.1894-227G>C rs34609268 0.05889
NM_025150.5(TARS2):c.387+199del rs3839012 0.04955
NM_025150.5(TARS2):c.81C>T (p.Thr27=) rs2275245 0.04914
NM_025150.5(TARS2):c.922-30G>T rs953127 0.04895
NM_025150.5(TARS2):c.*302A>G rs138986385 0.02965
NM_025150.5(TARS2):c.1401+17T>A rs12023021 0.02707
NM_025150.5(TARS2):c.388-174T>A rs115863890 0.02165
NM_025150.5(TARS2):c.66+136_66+139dup rs201661242 0.01829
NM_025150.5(TARS2):c.1197A>G (p.Thr399=) rs115388015 0.01495
NM_025150.5(TARS2):c.388-286C>G rs139648221 0.01491
NM_025150.5(TARS2):c.1820+41G>A rs77056123 0.01489
NM_025150.5(TARS2):c.1317C>T (p.Ala439=) rs116476409 0.01392
NM_025150.5(TARS2):c.1076C>T (p.Thr359Met) rs115720584 0.01145
NM_025150.5(TARS2):c.1034A>G (p.His345Arg) rs115390773 0.00560
NM_025150.5(TARS2):c.1251C>T (p.Ala417=) rs41264465 0.00537
NM_025150.5(TARS2):c.263+8G>T rs146092962 0.00491
NM_025150.5(TARS2):c.2103G>A (p.Gln701=) rs114661327 0.00467
NM_025150.5(TARS2):c.1453G>A (p.Val485Ile) rs116552645 0.00357
NM_025150.5(TARS2):c.513-282A>G rs77531603 0.00352
NM_025150.5(TARS2):c.-22G>A rs201336268 0.00340
NM_025150.5(TARS2):c.1160C>T (p.Pro387Leu) rs141179905 0.00202
NM_025150.5(TARS2):c.562C>A (p.Leu188Ile) rs140418026 0.00153
NM_025150.5(TARS2):c.1239-14C>T rs188574280 0.00122
NM_025150.5(TARS2):c.1719-20C>G rs587730315 0.00111
NM_025150.5(TARS2):c.1439G>A (p.Arg480His) rs148950017 0.00041
NM_025150.5(TARS2):c.1472G>A (p.Arg491His) rs145751121 0.00033
NM_025150.5(TARS2):c.1812G>C (p.Gly604=) rs144477069 0.00018
NM_025150.5(TARS2):c.366C>T (p.Phe122=) rs376600610 0.00011
NM_025150.5(TARS2):c.2142C>T (p.Ala714=) rs1042740553 0.00009
NM_025150.5(TARS2):c.1353G>A (p.Leu451=) rs776320671 0.00008
NM_025150.5(TARS2):c.49G>A (p.Ala17Thr) rs367864616 0.00008
NM_025150.5(TARS2):c.722A>G (p.Gln241Arg) rs182013142 0.00007
NM_025150.4(TARS2):c.-41C>T rs375885077 0.00006
NM_025150.5(TARS2):c.1131C>T (p.Ala377=) rs756982839 0.00004
NM_025150.5(TARS2):c.1756C>T (p.Arg586Ter) rs367870620 0.00004
NM_025150.5(TARS2):c.1768G>A (p.Gly590Ser) rs759043987 0.00004
NM_025150.5(TARS2):c.900G>C (p.Arg300=) rs775382225 0.00004
NM_025150.5(TARS2):c.1540-13C>T rs763390852 0.00002
NM_025150.5(TARS2):c.141A>G (p.Val47=) rs1274547718 0.00001
NM_025150.5(TARS2):c.933C>G (p.Leu311=) rs866255004 0.00001
NC_000001.11:g.150487218del rs3840449
NM_025150.4(TARS2):c.-31_-28del rs3840448
NM_025150.5(TARS2):c.*216dup rs72121396
NM_025150.5(TARS2):c.1020+15G>A rs1057521898
NM_025150.5(TARS2):c.1021-13C>A rs994932132
NM_025150.5(TARS2):c.1175A>T (p.Asp392Val)
NM_025150.5(TARS2):c.1301G>A (p.Gly434Glu)
NM_025150.5(TARS2):c.1375G>A (p.Ala459Thr)
NM_025150.5(TARS2):c.1617+168dup rs35689005
NM_025150.5(TARS2):c.1617+90dup rs34802685
NM_025150.5(TARS2):c.1618-25G>A rs4970927
NM_025150.5(TARS2):c.1719-15dup rs397690784
NM_025150.5(TARS2):c.1719-16C>A rs113876911
NM_025150.5(TARS2):c.1719-16C>T rs113876911
NM_025150.5(TARS2):c.1719-17C>A rs201218331
NM_025150.5(TARS2):c.1909C>T (p.Arg637Trp)
NM_025150.5(TARS2):c.191C>G (p.Ser64Ter)
NM_025150.5(TARS2):c.2053A>G (p.Thr685Ala)
NM_025150.5(TARS2):c.420G>T (p.Gly140=) rs1441723059
NM_025150.5(TARS2):c.513-10_513-8del rs587648372
NM_025150.5(TARS2):c.513-329_513-326del rs150477132
NM_025150.5(TARS2):c.513-330del rs66499095
NM_025150.5(TARS2):c.513-331_513-330dup rs66499095
NM_025150.5(TARS2):c.634A>G (p.Asn212Asp)
NM_025150.5(TARS2):c.695+142del rs111455328
NM_025150.5(TARS2):c.695+313_695+322del rs367685337
NM_025150.5(TARS2):c.695+320_695+322dup rs367685337
NM_025150.5(TARS2):c.695+321_695+322del rs367685337
NM_025150.5(TARS2):c.695+321_695+322dup rs367685337

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