ClinVar Miner

List of variants in gene ZNF423 studied for not provided

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Gene type:
ClinVar version:
Total variants: 91
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HGVS dbSNP gnomAD frequency
NM_001379286.1(ZNF423):c.3849+94T>G rs2287313 0.62317
NM_001379286.1(ZNF423):c.3849+53G>A rs2287314 0.60599
NM_001379286.1(ZNF423):c.101-66G>A rs2292155 0.39306
NM_001379286.1(ZNF423):c.40+32955C>G rs8060387 0.24790
NM_001379286.1(ZNF423):c.3601+55T>C rs16947716 0.11823
NM_001379286.1(ZNF423):c.100+159C>T rs2271063 0.11270
NM_001379286.1(ZNF423):c.3733+108G>A rs59065575 0.05696
NM_001379286.1(ZNF423):c.1569T>C (p.Asn523=) rs13336762 0.05236
NM_001379286.1(ZNF423):c.1910A>G (p.Asn637Ser) rs34214571 0.02773
NM_001379286.1(ZNF423):c.3850-23G>A rs12445683 0.02736
NM_001379286.1(ZNF423):c.3850-9C>T rs78514142 0.02527
NM_001379286.1(ZNF423):c.40+32859A>G rs7186878 0.02058
NM_001379286.1(ZNF423):c.3164C>T (p.Ala1055Val) rs111229124 0.00625
NM_001379286.1(ZNF423):c.1986C>T (p.His662=) rs75294107 0.00469
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.807C>T (p.Asp269=) rs145503941 0.00101
NM_001379286.1(ZNF423):c.3602-16C>T rs200838088 0.00099
NM_001379286.1(ZNF423):c.819C>T (p.Cys273=) rs201499268 0.00084
NM_001379286.1(ZNF423):c.3300C>T (p.Cys1100=) rs147816446 0.00073
NM_001379286.1(ZNF423):c.1168T>C (p.Ser390Pro) rs142835239 0.00063
NM_001379286.1(ZNF423):c.1677G>A (p.Pro559=) rs142344079 0.00061
NM_001379286.1(ZNF423):c.100+8C>T rs148101280 0.00041
NM_001379286.1(ZNF423):c.2312C>T (p.Ala771Val) rs150234048 0.00041
NM_001379286.1(ZNF423):c.2400C>T (p.Thr800=) rs151102991 0.00035
NM_001379286.1(ZNF423):c.2541C>T (p.Asn847=) rs146659313 0.00030
NM_001379286.1(ZNF423):c.3165G>A (p.Ala1055=) rs146700251 0.00029
NM_001379286.1(ZNF423):c.1848C>T (p.Ser616=) rs376218086 0.00023
NM_001379286.1(ZNF423):c.2683G>A (p.Gly895Ser) rs147413663 0.00019
NM_001379286.1(ZNF423):c.1132G>A (p.Ala378Thr) rs199760788 0.00011
NM_001379286.1(ZNF423):c.492C>T (p.His164=) rs550048605 0.00011
NM_001379286.1(ZNF423):c.146C>T (p.Ala49Val) rs147379553 0.00009
NM_001379286.1(ZNF423):c.1522C>T (p.Arg508Cys) rs376465155 0.00009
NM_001379286.1(ZNF423):c.2649C>T (p.Ser883=) rs781131703 0.00008
NM_001379286.1(ZNF423):c.2211C>T (p.Phe737=) rs138278000 0.00006
NM_001379286.1(ZNF423):c.2640T>C (p.His880=) rs200880737 0.00006
NM_001379286.1(ZNF423):c.1176G>A (p.Pro392=) rs748728165 0.00005
NM_001379286.1(ZNF423):c.1365G>C (p.Leu455=) rs548578929 0.00005
NM_001379286.1(ZNF423):c.3021C>T (p.Ser1007=) rs199536152 0.00005
NM_001379286.1(ZNF423):c.453C>T (p.Cys151=) rs569824346 0.00005
NM_001379286.1(ZNF423):c.2385G>A (p.Gly795=) rs189431522 0.00004
NM_001379286.1(ZNF423):c.2664C>T (p.Asp888=) rs376264701 0.00004
NM_001379286.1(ZNF423):c.3245G>A (p.Arg1082His) rs370797524 0.00004
NM_001379286.1(ZNF423):c.1217G>A (p.Arg406Gln) rs375001883 0.00003
NM_001379286.1(ZNF423):c.166G>A (p.Val56Met) rs772307020 0.00003
NM_001379286.1(ZNF423):c.2702C>T (p.Ala901Val) rs1051021187 0.00003
NM_001379286.1(ZNF423):c.3191A>G (p.Asn1064Ser) rs368041529 0.00003
NM_001379286.1(ZNF423):c.3301G>A (p.Ala1101Thr) rs144425413 0.00003
NM_001379286.1(ZNF423):c.2846C>T (p.Ser949Leu) rs778403528 0.00002
NM_001379286.1(ZNF423):c.1274G>A (p.Arg425Gln) rs150550744 0.00001
NM_001379286.1(ZNF423):c.1294G>A (p.Val432Met) rs375353056 0.00001
NM_001379286.1(ZNF423):c.1593C>T (p.Ser531=) rs1596763136 0.00001
NM_001379286.1(ZNF423):c.2276G>A (p.Arg759His) rs143285873 0.00001
NM_001379286.1(ZNF423):c.2480T>A (p.Ile827Asn) rs529454153 0.00001
NM_001379286.1(ZNF423):c.2548G>A (p.Ala850Thr) rs768539056 0.00001
NM_001379286.1(ZNF423):c.2589T>C (p.Pro863=) rs766758868 0.00001
NM_001379286.1(ZNF423):c.3467C>T (p.Pro1156Leu) rs756742718 0.00001
NM_001379286.1(ZNF423):c.410A>T (p.Glu137Val) rs886043664 0.00001
NM_001379286.1(ZNF423):c.504C>T (p.His168=) rs1328516403 0.00001
GRCh37/hg19 16q12.1(chr16:49469515-49961548)x3
GRCh37/hg19 16q12.1(chr16:49535643-49710372)x3
GRCh37/hg19 16q12.1(chr16:49796534-49837475)x3
NM_001379286.1(ZNF423):c.1022C>A (p.Ser341Tyr)
NM_001379286.1(ZNF423):c.1794C>T (p.Asn598=)
NM_001379286.1(ZNF423):c.1817A>G (p.Lys606Arg)
NM_001379286.1(ZNF423):c.2572A>C (p.Thr858Pro)
NM_001379286.1(ZNF423):c.2759G>A (p.Arg920Gln)
NM_001379286.1(ZNF423):c.2871G>A (p.Leu957=) rs1314213322
NM_001379286.1(ZNF423):c.2933C>T (p.Ser978Leu) rs794727731
NM_001379286.1(ZNF423):c.3106_3109del (p.Thr1036fs)
NM_001379286.1(ZNF423):c.3189dup (p.Asn1064fs) rs886041561
NM_001379286.1(ZNF423):c.3436C>G (p.His1146Asp)
NM_001379286.1(ZNF423):c.3556G>A (p.Glu1186Lys) rs771530800
NM_001379286.1(ZNF423):c.3630G>A (p.Leu1210=) rs1597050397
NM_001379286.1(ZNF423):c.3733+1G>A rs1567443640
NM_001379286.1(ZNF423):c.389G>T (p.Gly130Val) rs1064794776
NM_001379286.1(ZNF423):c.395A>G (p.Asp132Gly) rs2151888050
NM_001379286.1(ZNF423):c.411G>A (p.Glu137=) rs1596768180
NM_001379286.1(ZNF423):c.477C>T (p.Ser159=)
NM_001379286.1(ZNF423):c.495G>T (p.Glu165Asp) rs1972856533
NM_001379286.1(ZNF423):c.871C>A (p.Leu291Ile) rs770995307
NM_001379286.1(ZNF423):c.899A>C (p.Lys300Thr)

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