ClinVar Miner

List of variants in gene ZNF423 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_001379286.1(ZNF423):c.567T>C (p.Arg189=) rs3803665 0.55755
NM_001379286.1(ZNF423):c.2697T>C (p.Cys899=) rs3803667 0.21148
NM_001379286.1(ZNF423):c.1569T>C (p.Asn523=) rs13336762 0.05236
NM_001379286.1(ZNF423):c.1869G>A (p.Pro623=) rs16947741 0.02845
NM_001379286.1(ZNF423):c.1910A>G (p.Asn637Ser) rs34214571 0.02773
NM_001379286.1(ZNF423):c.3850-9C>T rs78514142 0.02527
NM_001379286.1(ZNF423):c.3351G>A (p.Pro1117=) rs113531514 0.01899
NM_001379286.1(ZNF423):c.3361G>A (p.Ala1121Thr) rs147898137 0.01162
NM_001379286.1(ZNF423):c.3164C>T (p.Ala1055Val) rs111229124 0.00625
NM_001379286.1(ZNF423):c.1194G>A (p.Pro398=) rs61747467 0.00494
NM_001379286.1(ZNF423):c.1986C>T (p.His662=) rs75294107 0.00469
NM_001379286.1(ZNF423):c.100+13G>A rs143660882 0.00463
NM_001379286.1(ZNF423):c.2562C>A (p.Pro854=) rs12599354 0.00459
NM_001379286.1(ZNF423):c.3291C>T (p.Tyr1097=) rs150027129 0.00408
NM_001379286.1(ZNF423):c.2328C>T (p.His776=) rs73565356 0.00402
NM_001379286.1(ZNF423):c.3226C>A (p.Leu1076Met) rs79706004 0.00398
NM_001379286.1(ZNF423):c.3393C>T (p.Pro1131=) rs61755180 0.00261
NM_001379286.1(ZNF423):c.2133G>A (p.Ser711=) rs143934881 0.00221
NM_001379286.1(ZNF423):c.3875A>C (p.Gln1292Pro) rs150302551 0.00213
NM_001379286.1(ZNF423):c.2013G>A (p.Ala671=) rs143468235 0.00207
NM_001379286.1(ZNF423):c.312C>T (p.Asp104=) rs117266679 0.00178
NM_001379286.1(ZNF423):c.1326G>A (p.Ala442=) rs16947743 0.00172
NM_001379286.1(ZNF423):c.1655G>T (p.Gly552Val) rs34425379 0.00158
NM_001379286.1(ZNF423):c.1560C>T (p.Asp520=) rs149371639 0.00073
NM_001379286.1(ZNF423):c.2006A>C (p.Lys669Thr) rs145272522 0.00049
NM_001379286.1(ZNF423):c.3180G>A (p.Ala1060=) rs117592972 0.00048
NM_001379286.1(ZNF423):c.100+8C>T rs148101280 0.00041
NM_001379286.1(ZNF423):c.1113C>T (p.Ser371=) rs149688169 0.00032
NM_001379286.1(ZNF423):c.1827C>T (p.Ala609=) rs376118736 0.00016
NM_001379286.1(ZNF423):c.615C>T (p.His205=) rs369646082 0.00014
NM_001379286.1(ZNF423):c.492C>T (p.His164=) rs550048605 0.00011
NM_001379286.1(ZNF423):c.1368C>T (p.Asp456=) rs146274919 0.00007
NM_001379286.1(ZNF423):c.2211C>T (p.Phe737=) rs138278000 0.00006
NM_001379286.1(ZNF423):c.2283G>A (p.Thr761=) rs758301410 0.00006
NM_001379286.1(ZNF423):c.1131C>T (p.Ser377=) rs369662414 0.00005
NM_001379286.1(ZNF423):c.2475C>T (p.His825=) rs201076539 0.00005
NM_001379286.1(ZNF423):c.2703G>A (p.Ala901=) rs140000430 0.00005
NM_001379286.1(ZNF423):c.2949C>T (p.Thr983=) rs748840936 0.00005
NM_001379286.1(ZNF423):c.2214C>T (p.Asp738=) rs147043161 0.00004
NM_001379286.1(ZNF423):c.2670G>A (p.Ser890=) rs369348426 0.00004
NM_001379286.1(ZNF423):c.3517-18T>C rs377719857 0.00004
NM_001379286.1(ZNF423):c.3739G>A (p.Val1247Ile) rs911470655 0.00004
NM_001379286.1(ZNF423):c.1230G>A (p.Gln410=) rs201769739 0.00003
NM_001379286.1(ZNF423):c.3702C>T (p.Gly1234=) rs766215720 0.00003
NM_001379286.1(ZNF423):c.426G>A (p.Thr142=) rs1040242592 0.00003
NM_001379286.1(ZNF423):c.1524C>T (p.Arg508=) rs756062396 0.00002
NM_001379286.1(ZNF423):c.231C>T (p.Cys77=) rs767825226 0.00002
NM_001379286.1(ZNF423):c.2952A>G (p.Glu984=) rs1288323161 0.00001
NM_001379286.1(ZNF423):c.3734-8G>T rs200126025 0.00001
NM_001379286.1(ZNF423):c.1176G>C (p.Pro392=) rs748728165
NM_001379286.1(ZNF423):c.2088G>A (p.Thr696=)
NM_001379286.1(ZNF423):c.2529T>C (p.Ala843=)
NM_001379286.1(ZNF423):c.2535C>T (p.Thr845=) rs77996576
NM_001379286.1(ZNF423):c.2769G>A (p.Glu923=) rs369901240
NM_001379286.1(ZNF423):c.3555C>T (p.Phe1185=)
NM_001379286.1(ZNF423):c.470G>A (p.Arg157His)
NM_001379286.1(ZNF423):c.49G>A (p.Gly17Arg)
NM_001379286.1(ZNF423):c.741C>T (p.Ser247=)

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