ClinVar Miner

List of variants in gene ZNF280C reported as uncertain significance for not specified

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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_017666.5(ZNF280C):c.1672A>C (p.Ser558Arg) rs369084123 0.00011
NM_017666.5(ZNF280C):c.1895C>T (p.Ala632Val) rs777740083 0.00010
NM_017666.5(ZNF280C):c.1790G>A (p.Arg597Gln) rs1162803764 0.00007
NM_017666.5(ZNF280C):c.689A>G (p.Asp230Gly) rs151127143 0.00007
NM_017666.5(ZNF280C):c.1795C>T (p.Arg599Cys) rs754326978 0.00006
NM_017666.5(ZNF280C):c.571A>G (p.Thr191Ala) rs1033204561 0.00005
NM_017666.5(ZNF280C):c.2102G>A (p.Arg701His) rs758892966 0.00004
NM_017666.5(ZNF280C):c.1898G>A (p.Ser633Asn) rs1200016835 0.00003
NM_017666.5(ZNF280C):c.1750A>G (p.Ile584Val) rs767391692 0.00002
NM_017666.5(ZNF280C):c.1133C>A (p.Pro378His) rs1331007823 0.00001
NM_017666.5(ZNF280C):c.1909A>G (p.Ile637Val) rs961526667 0.00001
NM_017666.5(ZNF280C):c.1060A>G (p.Thr354Ala)
NM_017666.5(ZNF280C):c.1271C>T (p.Thr424Ile) rs370269078
NM_017666.5(ZNF280C):c.1289C>G (p.Ala430Gly) rs2523239146
NM_017666.5(ZNF280C):c.1384A>T (p.Met462Leu) rs878873819
NM_017666.5(ZNF280C):c.1469C>T (p.Ala490Val)
NM_017666.5(ZNF280C):c.1625C>T (p.Pro542Leu)
NM_017666.5(ZNF280C):c.1628C>T (p.Thr543Ile) rs2523229844
NM_017666.5(ZNF280C):c.1635A>T (p.Gln545His)
NM_017666.5(ZNF280C):c.1700C>A (p.Ala567Glu)
NM_017666.5(ZNF280C):c.179A>C (p.Asn60Thr) rs779103852
NM_017666.5(ZNF280C):c.1982C>G (p.Ser661Cys)
NM_017666.5(ZNF280C):c.2005C>T (p.Arg669Trp)
NM_017666.5(ZNF280C):c.2092G>A (p.Gly698Ser) rs778134912
NM_017666.5(ZNF280C):c.2179A>G (p.Thr727Ala)
NM_017666.5(ZNF280C):c.2210A>C (p.Lys737Thr)
NM_017666.5(ZNF280C):c.256A>G (p.Ile86Val)
NM_017666.5(ZNF280C):c.278G>T (p.Arg93Leu) rs771031442
NM_017666.5(ZNF280C):c.288C>A (p.Asp96Glu) rs779156771
NM_017666.5(ZNF280C):c.464C>G (p.Ser155Cys)
NM_017666.5(ZNF280C):c.472A>G (p.Ile158Val)
NM_017666.5(ZNF280C):c.560A>G (p.Lys187Arg)
NM_017666.5(ZNF280C):c.566C>T (p.Pro189Leu)
NM_017666.5(ZNF280C):c.686A>G (p.Tyr229Cys)
NM_017666.5(ZNF280C):c.742C>G (p.Leu248Val) rs2523246956

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