ClinVar Miner

List of variants in gene ZNF462 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 91
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HGVS dbSNP gnomAD frequency
NM_021224.6(ZNF462):c.6013-143T>C rs41277827 0.00903
NM_021224.6(ZNF462):c.5328G>A (p.Ser1776=) rs17785570 0.00857
NC_000009.12:g.106860520T>G rs35277765 0.00517
NM_021224.6(ZNF462):c.441C>A (p.Ser147=) rs140067056 0.00331
NM_021224.6(ZNF462):c.238T>C (p.Leu80=) rs41277819 0.00046
NM_021224.6(ZNF462):c.5206A>G (p.Ile1736Val) rs192125496 0.00016
NM_021224.6(ZNF462):c.3481G>A (p.Glu1161Lys) rs746021945 0.00001
NM_021224.6(ZNF462):c.628G>A (p.Val210Ile) rs755534398 0.00001
NM_021224.6(ZNF462):c.1068A>G (p.Leu356=)
NM_021224.6(ZNF462):c.1076T>G (p.Leu359Trp)
NM_021224.6(ZNF462):c.1433C>A (p.Thr478Asn)
NM_021224.6(ZNF462):c.144C>T (p.Ser48=)
NM_021224.6(ZNF462):c.1485A>G (p.Thr495=)
NM_021224.6(ZNF462):c.1580G>A (p.Gly527Asp)
NM_021224.6(ZNF462):c.1608C>T (p.Pro536=)
NM_021224.6(ZNF462):c.1628C>T (p.Pro543Leu)
NM_021224.6(ZNF462):c.1643C>T (p.Pro548Leu)
NM_021224.6(ZNF462):c.1646C>T (p.Pro549Leu)
NM_021224.6(ZNF462):c.1648C>T (p.Pro550Ser)
NM_021224.6(ZNF462):c.1679_1696del (p.Leu560_Pro565del) rs747990150
NM_021224.6(ZNF462):c.1701_1715del (p.Gln567_Pro571del)
NM_021224.6(ZNF462):c.1782C>T (p.Ala594=)
NM_021224.6(ZNF462):c.1783G>A (p.Ala595Thr)
NM_021224.6(ZNF462):c.181T>A (p.Ser61Thr)
NM_021224.6(ZNF462):c.2121T>G (p.Ile707Met)
NM_021224.6(ZNF462):c.2196C>T (p.Val732=)
NM_021224.6(ZNF462):c.2263T>C (p.Phe755Leu) rs1830185151
NM_021224.6(ZNF462):c.2271C>G (p.Ala757=)
NM_021224.6(ZNF462):c.2283G>A (p.Trp761Ter)
NM_021224.6(ZNF462):c.2289A>G (p.Arg763=)
NM_021224.6(ZNF462):c.2437T>A (p.Ser813Thr)
NM_021224.6(ZNF462):c.3076A>G (p.Thr1026Ala)
NM_021224.6(ZNF462):c.3265A>G (p.Met1089Val)
NM_021224.6(ZNF462):c.3310C>A (p.Pro1104Thr)
NM_021224.6(ZNF462):c.3314C>T (p.Pro1105Leu)
NM_021224.6(ZNF462):c.3315G>A (p.Pro1105=)
NM_021224.6(ZNF462):c.3507A>C (p.Pro1169=)
NM_021224.6(ZNF462):c.3716G>A (p.Arg1239Gln)
NM_021224.6(ZNF462):c.3774C>T (p.Asp1258=)
NM_021224.6(ZNF462):c.3868G>A (p.Ala1290Thr)
NM_021224.6(ZNF462):c.4092C>T (p.Ala1364=)
NM_021224.6(ZNF462):c.4093G>A (p.Glu1365Lys)
NM_021224.6(ZNF462):c.410G>A (p.Gly137Glu)
NM_021224.6(ZNF462):c.4170A>G (p.Ala1390=)
NM_021224.6(ZNF462):c.4189A>C (p.Asn1397His)
NM_021224.6(ZNF462):c.4239G>A (p.Val1413=)
NM_021224.6(ZNF462):c.4389C>T (p.Pro1463=)
NM_021224.6(ZNF462):c.4446G>A (p.Leu1482=)
NM_021224.6(ZNF462):c.4601A>G (p.Tyr1534Cys)
NM_021224.6(ZNF462):c.4650C>T (p.His1550=)
NM_021224.6(ZNF462):c.4651G>A (p.Asp1551Asn)
NM_021224.6(ZNF462):c.4654G>A (p.Val1552Ile)
NM_021224.6(ZNF462):c.4749G>A (p.Pro1583=)
NM_021224.6(ZNF462):c.4784A>G (p.His1595Arg)
NM_021224.6(ZNF462):c.4789G>A (p.Glu1597Lys)
NM_021224.6(ZNF462):c.4827C>T (p.Ser1609=)
NM_021224.6(ZNF462):c.4853C>T (p.Pro1618Leu)
NM_021224.6(ZNF462):c.4864G>A (p.Glu1622Lys)
NM_021224.6(ZNF462):c.5013G>A (p.Thr1671=)
NM_021224.6(ZNF462):c.5114C>G (p.Thr1705Ser)
NM_021224.6(ZNF462):c.5244G>A (p.Pro1748=)
NM_021224.6(ZNF462):c.5397C>T (p.His1799=)
NM_021224.6(ZNF462):c.5472G>A (p.Glu1824=)
NM_021224.6(ZNF462):c.5531_5544del (p.Leu1844fs) rs2131515110
NM_021224.6(ZNF462):c.5665A>T (p.Asn1889Tyr)
NM_021224.6(ZNF462):c.5862A>G (p.Leu1954=)
NM_021224.6(ZNF462):c.6013-32G>A
NM_021224.6(ZNF462):c.6063C>T (p.Arg2021=)
NM_021224.6(ZNF462):c.6093G>A (p.Ser2031=)
NM_021224.6(ZNF462):c.6105T>C (p.Ala2035=)
NM_021224.6(ZNF462):c.623C>T (p.Pro208Leu)
NM_021224.6(ZNF462):c.6263_6268dup (p.Ser2089_Phe2090insCysSer)
NM_021224.6(ZNF462):c.627C>T (p.Pro209=)
NM_021224.6(ZNF462):c.6336C>T (p.Leu2112=)
NM_021224.6(ZNF462):c.6339C>T (p.Pro2113=)
NM_021224.6(ZNF462):c.633A>G (p.Ser211=)
NM_021224.6(ZNF462):c.6381C>G (p.His2127Gln)
NM_021224.6(ZNF462):c.6432A>G (p.Ser2144=)
NM_021224.6(ZNF462):c.6561T>C (p.Thr2187=)
NM_021224.6(ZNF462):c.6565G>C (p.Ala2189Pro)
NM_021224.6(ZNF462):c.6567C>T (p.Ala2189=)
NM_021224.6(ZNF462):c.6627T>C (p.His2209=)
NM_021224.6(ZNF462):c.6804C>T (p.Asn2268=)
NM_021224.6(ZNF462):c.6819C>T (p.Ile2273=)
NM_021224.6(ZNF462):c.6832+35G>A
NM_021224.6(ZNF462):c.6832+72C>T
NM_021224.6(ZNF462):c.819T>C (p.Leu273=)
NM_021224.6(ZNF462):c.838C>A (p.Gln280Lys)
NM_021224.6(ZNF462):c.863T>G (p.Val288Gly)
NM_021224.6(ZNF462):c.928C>T (p.Arg310Trp)
NM_021224.6(ZNF462):c.929G>A (p.Arg310Gln)

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