ClinVar Miner

List of variants in gene KDM5C reported as uncertain significance by Ambry Genetics

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_004187.5(KDM5C):c.3997T>G (p.Ser1333Ala) rs146572363 0.00016
NM_004187.5(KDM5C):c.1169G>A (p.Arg390Gln) rs1556849128 0.00003
NM_004187.5(KDM5C):c.652C>T (p.Pro218Ser) rs782076366 0.00003
NM_004187.5(KDM5C):c.3518G>A (p.Ser1173Asn) rs1556834744 0.00002
NM_004187.5(KDM5C):c.3668C>T (p.Pro1223Leu) rs199817424 0.00002
NM_004187.5(KDM5C):c.4406G>T (p.Gly1469Val) rs1428371887 0.00002
NM_004187.5(KDM5C):c.2830A>T (p.Arg944Trp) rs1018074229 0.00001
NM_004187.5(KDM5C):c.*124G>C
NM_004187.5(KDM5C):c.1054T>A (p.Phe352Ile)
NM_004187.5(KDM5C):c.1099C>T (p.Arg367Trp)
NM_004187.5(KDM5C):c.1393G>A (p.Glu465Lys)
NM_004187.5(KDM5C):c.1736A>G (p.His579Arg)
NM_004187.5(KDM5C):c.1837G>A (p.Glu613Lys) rs2073150409
NM_004187.5(KDM5C):c.1957G>A (p.Ala653Thr)
NM_004187.5(KDM5C):c.1988C>T (p.Ala663Val) rs1255690543
NM_004187.5(KDM5C):c.2165A>G (p.Tyr722Cys) rs1569264169
NM_004187.5(KDM5C):c.2366G>A (p.Arg789His)
NM_004187.5(KDM5C):c.2560C>T (p.Arg854Trp)
NM_004187.5(KDM5C):c.2663G>T (p.Arg888Leu) rs375850872
NM_004187.5(KDM5C):c.269C>T (p.Ala90Val) rs2073805082
NM_004187.5(KDM5C):c.3323C>T (p.Ala1108Val)
NM_004187.5(KDM5C):c.3526G>T (p.Ala1176Ser)
NM_004187.5(KDM5C):c.3755G>A (p.Arg1252His) rs1934666974
NM_004187.5(KDM5C):c.3961C>A (p.Pro1321Thr)
NM_004187.5(KDM5C):c.3962C>T (p.Pro1321Leu)
NM_004187.5(KDM5C):c.4040T>A (p.Val1347Asp) rs1569257275
NM_004187.5(KDM5C):c.4067G>A (p.Ser1356Asn)
NM_004187.5(KDM5C):c.4312C>G (p.Leu1438Val)
NM_004187.5(KDM5C):c.4381C>T (p.Arg1461Trp)
NM_004187.5(KDM5C):c.4399G>C (p.Gly1467Arg)
NM_004187.5(KDM5C):c.4483G>A (p.Glu1495Lys)
NM_004187.5(KDM5C):c.4511G>A (p.Gly1504Asp)
NM_004187.5(KDM5C):c.4649C>T (p.Pro1550Leu)
NM_004187.5(KDM5C):c.608C>T (p.Pro203Leu) rs797045641

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