ClinVar Miner

List of variants in gene ZNF423 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (1030):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 111
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HGVS dbSNP
NM_001271620.2(ZNF423):c.-131C>G rs1458377167
NM_001271620.2(ZNF423):c.-132G>A rs777866403
NM_001271620.2(ZNF423):c.-149C>T
NM_001271620.2(ZNF423):c.1013G>A (p.Arg338Gln)
NM_001271620.2(ZNF423):c.1070G>A (p.Arg357Gln) rs150550744
NM_001271620.2(ZNF423):c.1120G>A (p.Ala374Thr)
NM_001271620.2(ZNF423):c.1121C>T (p.Ala374Val)
NM_001271620.2(ZNF423):c.113C>G (p.Pro38Arg) rs113358702
NM_001271620.2(ZNF423):c.117A>G (p.Gln39=)
NM_001271620.2(ZNF423):c.1198G>A (p.Val400Ile)
NM_001271620.2(ZNF423):c.1208T>C (p.Leu403Pro) rs1596763863
NM_001271620.2(ZNF423):c.1291G>A (p.Asp431Asn) rs138661785
NM_001271620.2(ZNF423):c.1420G>A (p.Glu474Lys)
NM_001271620.2(ZNF423):c.1487C>G (p.Thr496Arg)
NM_001271620.2(ZNF423):c.1517C>T (p.Pro506Leu)
NM_001271620.2(ZNF423):c.158C>T (p.Ala53Val)
NM_001271620.2(ZNF423):c.1670G>A (p.Arg557Gln)
NM_001271620.2(ZNF423):c.167C>T (p.Thr56Met) rs376833288
NM_001271620.2(ZNF423):c.1684G>A (p.Ala562Thr)
NM_001271620.2(ZNF423):c.1690G>A (p.Ala564Thr)
NM_001271620.2(ZNF423):c.1690G>C (p.Ala564Pro) rs369619436
NM_001271620.2(ZNF423):c.1699A>G (p.Ile567Val)
NM_001271620.2(ZNF423):c.172A>G (p.Met58Val)
NM_001271620.2(ZNF423):c.1798C>T (p.Arg600Trp)
NM_001271620.2(ZNF423):c.1802A>C (p.Lys601Thr)
NM_001271620.2(ZNF423):c.1928C>T (p.Ser643Leu)
NM_001271620.2(ZNF423):c.2040G>A (p.Ala680=) rs186112147
NM_001271620.2(ZNF423):c.204C>T (p.Gly68=)
NM_001271620.2(ZNF423):c.2071C>T (p.Arg691Cys) rs757246232
NM_001271620.2(ZNF423):c.2108C>T (p.Ala703Val) rs150234048
NM_001271620.2(ZNF423):c.2327C>T (p.Ala776Val)
NM_001271620.2(ZNF423):c.2362A>G (p.Met788Val)
NM_001271620.2(ZNF423):c.2363T>C (p.Met788Thr) rs1596759188
NM_001271620.2(ZNF423):c.2404C>G (p.Leu802Val) rs774348975
NM_001271620.2(ZNF423):c.2461G>A (p.Ala821Thr)
NM_001271620.2(ZNF423):c.2465C>T (p.Ser822Leu) rs777639594
NM_001271620.2(ZNF423):c.2479G>A (p.Gly827Ser)
NM_001271620.2(ZNF423):c.2498C>T (p.Ala833Val) rs1051021187
NM_001271620.2(ZNF423):c.2499G>A (p.Ala833=) rs140000430
NM_001271620.2(ZNF423):c.250G>A (p.Asp84Asn)
NM_001271620.2(ZNF423):c.2558C>T (p.Pro853Leu) rs200585917
NM_001271620.2(ZNF423):c.2578C>T (p.Arg860Cys)
NM_001271620.2(ZNF423):c.2672C>T (p.Thr891Met)
NM_001271620.2(ZNF423):c.2780C>T (p.Thr927Met) rs143393771
NM_001271620.2(ZNF423):c.2814G>C (p.Gln938His)
NM_001271620.2(ZNF423):c.3005A>C (p.Lys1002Thr) rs1197947777
NM_001271620.2(ZNF423):c.3050A>G (p.Gln1017Arg) rs200494811
NM_001271620.2(ZNF423):c.3070G>A (p.Val1024Ile) rs759221881
NM_001271620.2(ZNF423):c.3100G>A (p.Gly1034Ser)
NM_001271620.2(ZNF423):c.3142G>C (p.Ala1048Pro)
NM_001271620.2(ZNF423):c.3169T>A (p.Cys1057Ser)
NM_001271620.2(ZNF423):c.3190G>A (p.Glu1064Lys) rs548986682
NM_001271620.2(ZNF423):c.3263C>T (p.Pro1088Leu) rs756742718
NM_001271620.2(ZNF423):c.3280C>T (p.Arg1094Trp)
NM_001271620.2(ZNF423):c.3487G>A (p.Glu1163Lys)
NM_001271620.2(ZNF423):c.3598G>A (p.Asp1200Asn) rs199688997
NM_001271620.2(ZNF423):c.3645+6T>A rs1340098894
NM_001271620.2(ZNF423):c.3646-3C>T
NM_001271620.2(ZNF423):c.508G>A (p.Gly170Ser) rs780153015
NM_001271620.2(ZNF423):c.601G>T (p.Asp201Tyr) rs569889555
NM_001271620.2(ZNF423):c.680C>T (p.Pro227Leu)
NM_001271620.2(ZNF423):c.775G>A (p.Ala259Thr)
NM_001271620.2(ZNF423):c.856C>T (p.Arg286Trp)
NM_001271620.2(ZNF423):c.865G>A (p.Asp289Asn) rs1045777723
NM_001271620.2(ZNF423):c.892G>A (p.Asp298Asn) rs760969654
NM_001271620.2(ZNF423):c.928G>A (p.Ala310Thr) rs199760788
NM_001271620.2(ZNF423):c.964T>C (p.Ser322Pro) rs142835239
NM_001379286.1(ZNF423):c.1124T>A (p.Met375Lys)
NM_001379286.1(ZNF423):c.1193C>T (p.Pro398Leu)
NM_001379286.1(ZNF423):c.1196T>C (p.Leu399Pro)
NM_001379286.1(ZNF423):c.1225G>A (p.Gly409Arg)
NM_001379286.1(ZNF423):c.1316C>G (p.Thr439Ser)
NM_001379286.1(ZNF423):c.1408A>G (p.Lys470Glu)
NM_001379286.1(ZNF423):c.1415A>G (p.His472Arg)
NM_001379286.1(ZNF423):c.1502A>G (p.Asn501Ser)
NM_001379286.1(ZNF423):c.1691C>T (p.Thr564Met)
NM_001379286.1(ZNF423):c.1693C>G (p.Gln565Glu)
NM_001379286.1(ZNF423):c.1873C>T (p.Arg625Trp)
NM_001379286.1(ZNF423):c.1880G>A (p.Arg627Gln)
NM_001379286.1(ZNF423):c.1886C>T (p.Ser629Leu)
NM_001379286.1(ZNF423):c.1964T>G (p.Phe655Cys)
NM_001379286.1(ZNF423):c.1978A>G (p.Lys660Glu)
NM_001379286.1(ZNF423):c.197A>C (p.Asp66Ala)
NM_001379286.1(ZNF423):c.2159T>C (p.Leu720Pro)
NM_001379286.1(ZNF423):c.2302C>T (p.Arg768Cys)
NM_001379286.1(ZNF423):c.2353C>G (p.Pro785Ala)
NM_001379286.1(ZNF423):c.2368A>G (p.Lys790Glu)
NM_001379286.1(ZNF423):c.2402A>G (p.Glu801Gly)
NM_001379286.1(ZNF423):c.2548G>A (p.Ala850Thr)
NM_001379286.1(ZNF423):c.2621C>T (p.Pro874Leu)
NM_001379286.1(ZNF423):c.2629C>T (p.Pro877Ser)
NM_001379286.1(ZNF423):c.2659G>A (p.Val887Met)
NM_001379286.1(ZNF423):c.2780C>T (p.Ser927Leu)
NM_001379286.1(ZNF423):c.2891C>G (p.Ala964Gly)
NM_001379286.1(ZNF423):c.296C>T (p.Pro99Leu)
NM_001379286.1(ZNF423):c.3085C>T (p.Arg1029Cys)
NM_001379286.1(ZNF423):c.313G>A (p.Asp105Asn)
NM_001379286.1(ZNF423):c.315C>A (p.Asp105Glu)
NM_001379286.1(ZNF423):c.3176C>T (p.Ala1059Val)
NM_001379286.1(ZNF423):c.317C>A (p.Pro106Gln)
NM_001379286.1(ZNF423):c.3244C>T (p.Arg1082Cys)
NM_001379286.1(ZNF423):c.327C>G (p.Ser109=)
NM_001379286.1(ZNF423):c.3316C>T (p.Arg1106Cys)
NM_001379286.1(ZNF423):c.3368G>A (p.Arg1123Gln)
NM_001379286.1(ZNF423):c.3775G>A (p.Val1259Met)
NM_001379286.1(ZNF423):c.40+33060A>C
NM_001379286.1(ZNF423):c.425C>T (p.Thr142Met)
NM_001379286.1(ZNF423):c.52G>C (p.Glu18Gln)
NM_001379286.1(ZNF423):c.848C>T (p.Thr283Met)
NM_001379286.1(ZNF423):c.877C>T (p.Arg293Cys)
NM_001379286.1(ZNF423):c.91A>G (p.Thr31Ala)

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