ClinVar Miner

List of variants in gene OR51B5 reported as uncertain significance by Ambry Genetics

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_001395252.1(OR51B5):c.434G>C (p.Gly145Ala) rs148591287 0.00016
NM_001395252.1(OR51B5):c.680C>T (p.Ala227Val) rs371637413 0.00011
NM_001395252.1(OR51B5):c.478C>T (p.Pro160Ser) rs201073099 0.00006
NM_001395252.1(OR51B5):c.829G>A (p.Ala277Thr) rs757159468 0.00005
NM_001395252.1(OR51B5):c.227T>C (p.Met76Thr) rs370740392 0.00003
NM_001395252.1(OR51B5):c.350C>T (p.Ala117Val) rs1848928074 0.00003
NM_001395252.1(OR51B5):c.556G>A (p.Ala186Thr) rs771737118 0.00003
NM_001395252.1(OR51B5):c.605T>C (p.Val202Ala) rs763132943 0.00003
NM_001395252.1(OR51B5):c.203A>G (p.Asp68Gly) rs763376441 0.00002
NM_001395252.1(OR51B5):c.416T>G (p.Val139Gly) rs767734992 0.00002
NM_001395252.1(OR51B5):c.502C>T (p.His168Tyr) rs767661897 0.00002
NM_001395252.1(OR51B5):c.226A>G (p.Met76Val) rs747190967 0.00001
NM_001395252.1(OR51B5):c.761T>C (p.Ile254Thr) rs771089918 0.00001
NM_001395252.1(OR51B5):c.904C>G (p.Leu302Val) rs773359755 0.00001
NM_001395252.1(OR51B5):c.143A>T (p.Lys48Met)
NM_001395252.1(OR51B5):c.204C>G (p.Asp68Glu) rs546965603
NM_001395252.1(OR51B5):c.214G>T (p.Ala72Ser) rs2494419095
NM_001395252.1(OR51B5):c.227T>A (p.Met76Lys)
NM_001395252.1(OR51B5):c.264G>T (p.Arg88Ser)
NM_001395252.1(OR51B5):c.266A>C (p.Glu89Ala)
NM_001395252.1(OR51B5):c.284G>T (p.Cys95Phe) rs61738484
NM_001395252.1(OR51B5):c.301T>C (p.Phe101Leu) rs1286534067
NM_001395252.1(OR51B5):c.303T>A (p.Phe101Leu)
NM_001395252.1(OR51B5):c.317C>G (p.Ser106Cys) rs1435926857
NM_001395252.1(OR51B5):c.332G>C (p.Gly111Ala) rs1589942099
NM_001395252.1(OR51B5):c.370A>G (p.Ile124Val)
NM_001395252.1(OR51B5):c.376A>T (p.Asn126Tyr)
NM_001395252.1(OR51B5):c.413G>A (p.Arg138Gln) rs547271833
NM_001395252.1(OR51B5):c.488T>A (p.Phe163Tyr)
NM_001395252.1(OR51B5):c.5C>T (p.Ser2Leu)
NM_001395252.1(OR51B5):c.64C>T (p.His22Tyr)
NM_001395252.1(OR51B5):c.707T>C (p.Leu236Pro) rs1848918438

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