ClinVar Miner

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

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP
NM_001271620.2(ZNF423):c.-131C>G
NM_001271620.2(ZNF423):c.-132G>A
NM_001271620.2(ZNF423):c.1070G>A (p.Arg357Gln)
NM_001271620.2(ZNF423):c.113C>G (p.Pro38Arg)
NM_001271620.2(ZNF423):c.1208T>C (p.Leu403Pro)
NM_001271620.2(ZNF423):c.1291G>A (p.Asp431Asn) rs138661785
NM_001271620.2(ZNF423):c.167C>T (p.Thr56Met) rs376833288
NM_001271620.2(ZNF423):c.1690G>C (p.Ala564Pro)
NM_001271620.2(ZNF423):c.2040G>A (p.Ala680=) rs186112147
NM_001271620.2(ZNF423):c.2071C>T (p.Arg691Cys)
NM_001271620.2(ZNF423):c.2363T>C (p.Met788Thr)
NM_001271620.2(ZNF423):c.2404C>G (p.Leu802Val) rs774348975
NM_001271620.2(ZNF423):c.2465C>T (p.Ser822Leu)
NM_001271620.2(ZNF423):c.2780C>T (p.Thr927Met)
NM_001271620.2(ZNF423):c.3005A>C (p.Lys1002Thr)
NM_001271620.2(ZNF423):c.3050A>G (p.Gln1017Arg)
NM_001271620.2(ZNF423):c.3263C>T (p.Pro1088Leu) rs756742718
NM_001271620.2(ZNF423):c.3598G>A (p.Asp1200Asn)
NM_001271620.2(ZNF423):c.3645+6T>A
NM_001271620.2(ZNF423):c.508G>A (p.Gly170Ser)
NM_001271620.2(ZNF423):c.601G>T (p.Asp201Tyr)
NM_001271620.2(ZNF423):c.865G>A (p.Asp289Asn) rs1045777723
NM_001271620.2(ZNF423):c.892G>A (p.Asp298Asn)
NM_001271620.2(ZNF423):c.964T>C (p.Ser322Pro) rs142835239

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