ClinVar Miner

List of variants in gene TARS2 reported as likely benign by GeneDx

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_025150.5(TARS2):c.388-286C>G rs139648221 0.01491
NM_025150.5(TARS2):c.1251C>T (p.Ala417=) rs41264465 0.00537
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.1239-14C>T rs188574280 0.00122
NM_025150.5(TARS2):c.1719-20C>G rs587730315 0.00111
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.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.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
NM_025150.5(TARS2):c.1020+15G>A rs1057521898
NM_025150.5(TARS2):c.1021-13C>A rs994932132
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.420G>T (p.Gly140=) rs1441723059
NM_025150.5(TARS2):c.513-10_513-8del rs587648372

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