ClinVar Miner

List of variants in gene ZNF407 reported as uncertain significance for not specified

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Gene type:
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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_017757.3(ZNF407):c.1991G>T (p.Ser664Ile) rs149806516 0.00286
NM_017757.3(ZNF407):c.5589G>A (p.Val1863=) rs183815209 0.00125
NM_017757.3(ZNF407):c.6077A>G (p.Gln2026Arg) rs202203566 0.00084
NM_017757.3(ZNF407):c.5737G>A (p.Ala1913Thr) rs17056248 0.00029
NM_017757.3(ZNF407):c.*3C>T rs189222961 0.00026
NM_017757.3(ZNF407):c.6301G>A (p.Gly2101Ser) rs200271129 0.00024
NM_017757.3(ZNF407):c.1526C>T (p.Pro509Leu) rs376677482 0.00015
NM_017757.3(ZNF407):c.4758G>A (p.Val1586=) rs371417079 0.00015
NM_017757.3(ZNF407):c.6697G>A (p.Ala2233Thr) rs377200520 0.00014
NM_017757.3(ZNF407):c.5936G>A (p.Gly1979Glu) rs542110142 0.00011
NM_017757.3(ZNF407):c.5718G>A (p.Thr1906=) rs754942254 0.00007
NM_017757.3(ZNF407):c.1664T>C (p.Met555Thr) rs527983284 0.00006
NM_017757.3(ZNF407):c.6526C>T (p.Pro2176Ser) rs371338916 0.00006
NM_017757.3(ZNF407):c.*5C>T rs1022719683 0.00004
NM_017757.3(ZNF407):c.1600G>A (p.Gly534Arg) rs781554422 0.00004
NM_017757.3(ZNF407):c.4866C>T (p.Thr1622=) rs752545983 0.00004
NM_017757.3(ZNF407):c.6283G>A (p.Gly2095Ser) rs112370735 0.00004
NM_017757.3(ZNF407):c.1519C>T (p.Arg507Cys) rs780972850 0.00003
NM_017757.3(ZNF407):c.1530C>T (p.Asp510=) rs373519575 0.00003
NM_017757.3(ZNF407):c.1296C>T (p.Ser432=) rs372418170 0.00001
NM_017757.3(ZNF407):c.3586A>G (p.Ser1196Gly) rs199680209 0.00001
NM_017757.3(ZNF407):c.3649C>T (p.His1217Tyr) rs776425129 0.00001
NM_017757.3(ZNF407):c.3660G>A (p.Ser1220=) rs768043004 0.00001
NM_017757.3(ZNF407):c.3773G>A (p.Arg1258His) rs747340041 0.00001
NM_017757.3(ZNF407):c.5631C>T (p.Ala1877=) rs778815168 0.00001
NM_017757.3(ZNF407):c.6153C>T (p.Ala2051=) rs373080209 0.00001
NM_017757.3(ZNF407):c.1448G>C (p.Cys483Ser) rs776451413
NM_017757.3(ZNF407):c.2021C>T (p.Ser674Phe) rs1555670651
NM_017757.3(ZNF407):c.2235C>T (p.Ser745=) rs797046126
NM_017757.3(ZNF407):c.266A>G (p.Gln89Arg)
NM_017757.3(ZNF407):c.4653G>A (p.Ser1551=) rs774684426
NM_017757.3(ZNF407):c.4662C>T (p.Phe1554=) rs797046128
NM_017757.3(ZNF407):c.4795G>A (p.Val1599Ile) rs2144688984
NM_017757.3(ZNF407):c.5334T>C (p.Cys1778=) rs772099571
NM_017757.3(ZNF407):c.5863G>A (p.Glu1955Lys) rs777049090
NM_017757.3(ZNF407):c.6734T>C (p.Leu2245Pro) rs370159868
NM_017757.3(ZNF407):c.94G>T (p.Asp32Tyr) rs754424061

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