ClinVar Miner

List of variants in gene OR2A25 reported as uncertain significance

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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_001386096.1(OR2A25):c.370G>A (p.Ala124Thr) rs370425216 0.00027
NM_001386096.1(OR2A25):c.474T>G (p.His158Gln) rs376429492 0.00021
NM_001386096.1(OR2A25):c.547G>T (p.Val183Phe) rs200681773 0.00020
NM_001386096.1(OR2A25):c.664T>C (p.Cys222Arg) rs371363692 0.00013
NM_001386096.1(OR2A25):c.265A>G (p.Lys89Glu) rs199712223 0.00009
NM_001386096.1(OR2A25):c.323A>G (p.His108Arg) rs202092146 0.00005
NM_001386096.1(OR2A25):c.871C>T (p.Leu291Phe) rs376525259 0.00003
NM_001386096.1(OR2A25):c.451G>A (p.Gly151Arg) rs201188715 0.00002
NM_001386096.1(OR2A25):c.925A>T (p.Thr309Ser) rs778095371 0.00002
NM_001386096.1(OR2A25):c.608T>C (p.Val203Ala) rs2051099149 0.00001
NM_001386096.1(OR2A25):c.776T>C (p.Val259Ala) rs2051101700 0.00001
NM_001386096.1(OR2A25):c.128C>T (p.Thr43Ile)
NM_001386096.1(OR2A25):c.211G>C (p.Ala71Pro) rs756605755
NM_001386096.1(OR2A25):c.221G>A (p.Cys74Tyr)
NM_001386096.1(OR2A25):c.236A>G (p.Gln79Arg) rs201927844
NM_001386096.1(OR2A25):c.258T>A (p.His86Gln)
NM_001386096.1(OR2A25):c.286T>C (p.Cys96Arg)
NM_001386096.1(OR2A25):c.328G>C (p.Glu110Gln) rs2051094528
NM_001386096.1(OR2A25):c.356A>G (p.Tyr119Cys)
NM_001386096.1(OR2A25):c.419G>T (p.Cys140Phe)
NM_001386096.1(OR2A25):c.421A>C (p.Ile141Leu)
NM_001386096.1(OR2A25):c.521A>G (p.Asn174Ser) rs2485634312
NM_001386096.1(OR2A25):c.53T>C (p.Ile18Thr)
NM_001386096.1(OR2A25):c.590T>A (p.Met197Lys) rs201803639
NM_001386096.1(OR2A25):c.592G>C (p.Val198Leu)
NM_001386096.1(OR2A25):c.665G>T (p.Cys222Phe) rs758409645
NM_001386096.1(OR2A25):c.730C>T (p.Leu244Phe)
NM_001386096.1(OR2A25):c.746T>G (p.Leu249Arg)
NM_001386096.1(OR2A25):c.839T>C (p.Phe280Ser) rs2485635040
NM_001386096.1(OR2A25):c.899T>C (p.Leu300Pro)

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