ClinVar Miner

List of variants in gene ZNF510 reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_014930.3(ZNF510):c.1975A>C (p.Asn659His) rs150643136 0.00033
NM_014930.3(ZNF510):c.1328A>G (p.Gln443Arg) rs139940378 0.00032
NM_014930.3(ZNF510):c.1149G>T (p.Lys383Asn) rs139454408 0.00017
NM_014930.3(ZNF510):c.1402A>G (p.Thr468Ala) rs768660889 0.00017
NM_014930.3(ZNF510):c.1993T>C (p.Cys665Arg) rs138235342 0.00015
NM_014930.3(ZNF510):c.1387A>C (p.Asn463His) rs147329007 0.00013
NM_014930.3(ZNF510):c.1180C>T (p.Arg394Cys) rs371685073 0.00012
NM_014930.3(ZNF510):c.1840A>G (p.Ile614Val) rs147318678 0.00009
NM_014930.3(ZNF510):c.1832G>A (p.Arg611Gln) rs201666879 0.00007
NM_014930.3(ZNF510):c.22A>G (p.Ile8Val) rs201603140 0.00007
NM_014930.3(ZNF510):c.1163C>T (p.Thr388Met) rs554451874 0.00006
NM_014930.3(ZNF510):c.1748G>A (p.Arg583Gln) rs140977740 0.00004
NM_014930.3(ZNF510):c.1957G>A (p.Glu653Lys) rs766200811 0.00002
NM_014930.3(ZNF510):c.41T>C (p.Leu14Pro) rs745420848 0.00002
NM_014930.3(ZNF510):c.950C>T (p.Ser317Phe) rs749771699 0.00002
NM_014930.3(ZNF510):c.1087C>A (p.Pro363Thr) rs773758294 0.00001
NM_014930.3(ZNF510):c.1144A>T (p.Asn382Tyr) rs1271539950 0.00001
NM_014930.3(ZNF510):c.1523G>A (p.Arg508Lys) rs763036488 0.00001
NM_014930.3(ZNF510):c.1747C>T (p.Arg583Trp) rs765526190 0.00001
NM_014930.3(ZNF510):c.1756A>G (p.Thr586Ala) rs1326648474 0.00001
NM_014930.3(ZNF510):c.419C>A (p.Ala140Glu) rs763359345 0.00001
NM_014930.3(ZNF510):c.683A>C (p.His228Pro) rs371093613 0.00001
NM_014930.3(ZNF510):c.728A>T (p.Lys243Met) rs776302544 0.00001
NM_014930.3(ZNF510):c.783A>C (p.Lys261Asn) rs779275104 0.00001
NM_014930.3(ZNF510):c.1166C>G (p.Ser389Trp)
NM_014930.3(ZNF510):c.1171C>G (p.His391Asp)
NM_014930.3(ZNF510):c.1217G>A (p.Cys406Tyr) rs754787077
NM_014930.3(ZNF510):c.1268A>G (p.Gln423Arg)
NM_014930.3(ZNF510):c.1318A>G (p.Thr440Ala)
NM_014930.3(ZNF510):c.1421C>T (p.Thr474Ile)
NM_014930.3(ZNF510):c.1478G>A (p.Cys493Tyr)
NM_014930.3(ZNF510):c.1537G>A (p.Glu513Lys)
NM_014930.3(ZNF510):c.1605G>C (p.Gln535His) rs1849273640
NM_014930.3(ZNF510):c.1622A>G (p.Glu541Gly) rs2539670681
NM_014930.3(ZNF510):c.1628C>G (p.Thr543Ser) rs141487263
NM_014930.3(ZNF510):c.1660T>C (p.Trp554Arg)
NM_014930.3(ZNF510):c.1664G>A (p.Arg555Gln)
NM_014930.3(ZNF510):c.1682A>G (p.Gln561Arg)
NM_014930.3(ZNF510):c.1715T>G (p.Phe572Cys)
NM_014930.3(ZNF510):c.1721G>C (p.Cys574Ser) rs376290596
NM_014930.3(ZNF510):c.1864C>T (p.His622Tyr)
NM_014930.3(ZNF510):c.2013C>A (p.Ser671Arg)
NM_014930.3(ZNF510):c.207T>G (p.Asn69Lys)
NM_014930.3(ZNF510):c.247G>A (p.Val83Ile)
NM_014930.3(ZNF510):c.250T>C (p.Ser84Pro)
NM_014930.3(ZNF510):c.337A>C (p.Asn113His) rs1849391853
NM_014930.3(ZNF510):c.499G>A (p.Val167Ile)
NM_014930.3(ZNF510):c.557T>C (p.Ile186Thr)
NM_014930.3(ZNF510):c.593C>G (p.Thr198Arg) rs2539675161
NM_014930.3(ZNF510):c.617T>C (p.Val206Ala) rs1387472303
NM_014930.3(ZNF510):c.76C>A (p.Pro26Thr) rs1849656408
NM_014930.3(ZNF510):c.82C>T (p.Arg28Trp)
NM_014930.3(ZNF510):c.848A>G (p.Lys283Arg)
NM_014930.3(ZNF510):c.88T>A (p.Ser30Thr)
NM_014930.3(ZNF510):c.91A>G (p.Thr31Ala)
NM_014930.3(ZNF510):c.946A>G (p.Lys316Glu) rs1588125651
NM_014930.3(ZNF510):c.94C>A (p.Leu32Ile) rs748614843
NM_014930.3(ZNF510):c.955G>C (p.Glu319Gln) rs1564434268

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