ClinVar Miner

List of variants in gene TAAR2 reported as uncertain significance

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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_001033080.1(TAAR2):c.658A>G (p.Thr220Ala) rs61731217 0.00028
NM_001033080.1(TAAR2):c.729C>G (p.Ile243Met) rs368292716 0.00021
NM_001033080.1(TAAR2):c.407C>T (p.Ser136Leu) rs142577385 0.00020
NM_001033080.1(TAAR2):c.942A>G (p.Ile314Met) rs372803383 0.00013
NM_001033080.1(TAAR2):c.133G>A (p.Ala45Thr) rs202050977 0.00012
NM_001033080.1(TAAR2):c.943T>C (p.Tyr315His) rs200471202 0.00011
NM_001033080.1(TAAR2):c.740G>A (p.Arg247Gln) rs772848812 0.00009
NM_001033080.1(TAAR2):c.335G>A (p.Gly112Glu) rs369503456 0.00008
NM_001033080.1(TAAR2):c.533T>A (p.Val178Glu) rs141239990 0.00004
NM_001033080.1(TAAR2):c.1025C>A (p.Thr342Asn) rs1444823600 0.00001
NM_001033080.1(TAAR2):c.158C>T (p.Ser53Phe) rs1389203364 0.00001
NM_001033080.1(TAAR2):c.668C>A (p.Ser223Tyr) rs770782356 0.00001
NM_001033080.1(TAAR2):c.731A>G (p.Asn244Ser) rs375499103 0.00001
NM_001033080.1(TAAR2):c.935C>T (p.Pro312Leu) rs746705772 0.00001
NM_001033080.1(TAAR2):c.1012T>C (p.Cys338Arg) rs2483189362
NM_001033080.1(TAAR2):c.121G>C (p.Gly41Arg)
NM_001033080.1(TAAR2):c.182A>G (p.Asn61Ser)
NM_001033080.1(TAAR2):c.194T>C (p.Ile65Thr)
NM_001033080.1(TAAR2):c.284C>T (p.Thr95Ile)
NM_001033080.1(TAAR2):c.301A>G (p.Met101Val) rs2483192936
NM_001033080.1(TAAR2):c.311C>G (p.Ser104Trp) rs550125345
NM_001033080.1(TAAR2):c.349A>G (p.Lys117Glu)
NM_001033080.1(TAAR2):c.382A>G (p.Ile128Val) rs773819525
NM_001033080.1(TAAR2):c.569G>T (p.Gly190Val)
NM_001033080.1(TAAR2):c.582G>C (p.Leu194Phe)
NM_001033080.1(TAAR2):c.596G>T (p.Ser199Ile)
NM_001033080.1(TAAR2):c.611T>C (p.Met204Thr) rs751950255
NM_001033080.1(TAAR2):c.642T>G (p.Phe214Leu) rs1378899435
NM_001033080.1(TAAR2):c.676G>A (p.Val226Met) rs1237920142
NM_001033080.1(TAAR2):c.716A>G (p.His239Arg) rs376107701
NM_001033080.1(TAAR2):c.772A>C (p.Lys258Gln) rs746428524
NM_001033080.1(TAAR2):c.772A>G (p.Lys258Glu)
NM_001033080.1(TAAR2):c.833G>A (p.Cys278Tyr)
NM_001033080.1(TAAR2):c.859T>C (p.Phe287Leu) rs1296881171
NM_001033080.1(TAAR2):c.967C>T (p.Arg323Cys)

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