ClinVar Miner

List of variants in gene ZNF423 studied for abdominal and pelvic region disorder

Included ClinVar conditions (961):
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Gene type:
ClinVar version:
Total variants: 128
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HGVS dbSNP
NM_001271620.2(ZNF423):c.-105+10C>T
NM_001271620.2(ZNF423):c.-105+8C>T
NM_001271620.2(ZNF423):c.-118C>T rs116537749
NM_001271620.2(ZNF423):c.-131C>G
NM_001271620.2(ZNF423):c.-132G>A
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)
NM_001271620.2(ZNF423):c.108C>T (p.Asp36=) rs117266679
NM_001271620.2(ZNF423):c.1120G>A (p.Ala374Thr)
NM_001271620.2(ZNF423):c.1121C>T (p.Ala374Val)
NM_001271620.2(ZNF423):c.1122G>A (p.Ala374=) rs16947743
NM_001271620.2(ZNF423):c.113C>G (p.Pro38Arg) rs113358702
NM_001271620.2(ZNF423):c.1164C>T (p.Asp388=)
NM_001271620.2(ZNF423):c.117A>G (p.Gln39=)
NM_001271620.2(ZNF423):c.1197C>T (p.His399=) rs370346450
NM_001271620.2(ZNF423):c.1198G>A (p.Val400Ile)
NM_001271620.2(ZNF423):c.1208T>C (p.Leu403Pro)
NM_001271620.2(ZNF423):c.1257C>T (p.Ala419=)
NM_001271620.2(ZNF423):c.1291G>A (p.Asp431Asn) rs138661785
NM_001271620.2(ZNF423):c.1338del (p.Asn447fs)
NM_001271620.2(ZNF423):c.1356C>T (p.Asp452=) rs149371639
NM_001271620.2(ZNF423):c.1357G>A (p.Gly453Ser)
NM_001271620.2(ZNF423):c.1365T>C (p.Asn455=) rs13336762
NM_001271620.2(ZNF423):c.1420G>A (p.Glu474Lys)
NM_001271620.2(ZNF423):c.1451G>T (p.Gly484Val) rs34425379
NM_001271620.2(ZNF423):c.1473G>A (p.Pro491=)
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.159G>A (p.Ala53=)
NM_001271620.2(ZNF423):c.1644C>T (p.Ser548=)
NM_001271620.2(ZNF423):c.1665G>A (p.Pro555=) rs16947741
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.1689C>T (p.Ser563=) rs151294188
NM_001271620.2(ZNF423):c.1690G>A (p.Ala564Thr)
NM_001271620.2(ZNF423):c.1690G>C (p.Ala564Pro)
NM_001271620.2(ZNF423):c.1699A>G (p.Ile567Val)
NM_001271620.2(ZNF423):c.1706A>G (p.Asn569Ser) rs34214571
NM_001271620.2(ZNF423):c.172A>G (p.Met58Val)
NM_001271620.2(ZNF423):c.1782C>T (p.His594=) rs75294107
NM_001271620.2(ZNF423):c.1798C>T (p.Arg600Trp)
NM_001271620.2(ZNF423):c.1802A>C (p.Lys601Thr)
NM_001271620.2(ZNF423):c.1809G>A (p.Ala603=) rs143468235
NM_001271620.2(ZNF423):c.1902C>T (p.Cys634=) rs760404444
NM_001271620.2(ZNF423):c.1928C>T (p.Ser643Leu)
NM_001271620.2(ZNF423):c.1929G>A (p.Ser643=) rs143934881
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)
NM_001271620.2(ZNF423):c.2124C>T (p.His708=) rs73565356
NM_001271620.2(ZNF423):c.222G>A (p.Thr74=)
NM_001271620.2(ZNF423):c.2327C>T (p.Ala776Val)
NM_001271620.2(ZNF423):c.2331C>T (p.Thr777=) rs77996576
NM_001271620.2(ZNF423):c.2337C>T (p.Asn779=)
NM_001271620.2(ZNF423):c.2351G>A (p.Gly784Glu)
NM_001271620.2(ZNF423):c.2358C>A (p.Pro786=) rs12599354
NM_001271620.2(ZNF423):c.2362A>G (p.Met788Val)
NM_001271620.2(ZNF423):c.2363T>C (p.Met788Thr)
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.250G>A (p.Asp84Asn)
NM_001271620.2(ZNF423):c.2558C>T (p.Pro853Leu) rs200585917
NM_001271620.2(ZNF423):c.2577A>G (p.Ser859=) rs1555514937
NM_001271620.2(ZNF423):c.2578C>T (p.Arg860Cys)
NM_001271620.2(ZNF423):c.2643G>A (p.Ser881=)
NM_001271620.2(ZNF423):c.2672C>T (p.Thr891Met)
NM_001271620.2(ZNF423):c.2739G>A (p.Thr913=)
NM_001271620.2(ZNF423):c.2780C>T (p.Thr927Met)
NM_001271620.2(ZNF423):c.2808C>G (p.Pro936=)
NM_001271620.2(ZNF423):c.2814G>C (p.Gln938His)
NM_001271620.2(ZNF423):c.2857C>T (p.Leu953=) rs35529066
NM_001271620.2(ZNF423):c.288C>T (p.His96=)
NM_001271620.2(ZNF423):c.2960C>T (p.Ala987Val) rs111229124
NM_001271620.2(ZNF423):c.2961G>A (p.Ala987=)
NM_001271620.2(ZNF423):c.2976G>A (p.Ala992=) rs117592972
NM_001271620.2(ZNF423):c.3005A>C (p.Lys1002Thr)
NM_001271620.2(ZNF423):c.3022C>A (p.Leu1008Met) rs79706004
NM_001271620.2(ZNF423):c.3050A>G (p.Gln1017Arg) rs200494811
NM_001271620.2(ZNF423):c.3070G>A (p.Val1024Ile)
NM_001271620.2(ZNF423):c.3087C>T (p.Tyr1029=) rs150027129
NM_001271620.2(ZNF423):c.3096C>T (p.Cys1032=) rs147816446
NM_001271620.2(ZNF423):c.3099C>T (p.Ala1033=)
NM_001271620.2(ZNF423):c.3100G>A (p.Gly1034Ser)
NM_001271620.2(ZNF423):c.3132G>A (p.Val1044=) rs61739947
NM_001271620.2(ZNF423):c.3142G>C (p.Ala1048Pro)
NM_001271620.2(ZNF423):c.3147G>A (p.Pro1049=) rs113531514
NM_001271620.2(ZNF423):c.3157G>A (p.Ala1053Thr) rs147898137
NM_001271620.2(ZNF423):c.3169T>A (p.Cys1057Ser)
NM_001271620.2(ZNF423):c.3174C>T (p.Ala1058=)
NM_001271620.2(ZNF423):c.3189C>T (p.Pro1063=) rs61755180
NM_001271620.2(ZNF423):c.3216C>T (p.Ala1072=)
NM_001271620.2(ZNF423):c.3263C>T (p.Pro1088Leu) rs756742718
NM_001271620.2(ZNF423):c.3280C>T (p.Arg1094Trp)
NM_001271620.2(ZNF423):c.3486C>T (p.Phe1162=)
NM_001271620.2(ZNF423):c.3487G>A (p.Glu1163Lys)
NM_001271620.2(ZNF423):c.3552G>A (p.Leu1184=) rs762410542
NM_001271620.2(ZNF423):c.3597C>T (p.Tyr1199=)
NM_001271620.2(ZNF423):c.3598G>A (p.Asp1200Asn)
NM_001271620.2(ZNF423):c.3636C>T (p.Thr1212=)
NM_001271620.2(ZNF423):c.3645+6T>A
NM_001271620.2(ZNF423):c.3646-3C>T
NM_001271620.2(ZNF423):c.3646-9C>T rs78514142
NM_001271620.2(ZNF423):c.3649C>T (p.His1217Tyr)
NM_001271620.2(ZNF423):c.3671A>C (p.Gln1224Pro)
NM_001271620.2(ZNF423):c.414G>A (p.Glu138=) rs1555516039
NM_001271620.2(ZNF423):c.426C>T (p.Ala142=)
NM_001271620.2(ZNF423):c.507C>T (p.Arg169=) rs16947744
NM_001271620.2(ZNF423):c.508G>A (p.Gly170Ser)
NM_001271620.2(ZNF423):c.601G>T (p.Asp201Tyr)
NM_001271620.2(ZNF423):c.603C>T (p.Asp201=) rs145503941
NM_001271620.2(ZNF423):c.615C>T (p.Cys205=) rs201499268
NM_001271620.2(ZNF423):c.680C>T (p.Pro227Leu)
NM_001271620.2(ZNF423):c.69G>A (p.Thr23=)
NM_001271620.2(ZNF423):c.775G>A (p.Ala259Thr)
NM_001271620.2(ZNF423):c.856C>T (p.Arg286Trp)
NM_001271620.2(ZNF423):c.864C>T (p.Pro288=)
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.909C>T (p.Ser303=)
NM_001271620.2(ZNF423):c.928G>A (p.Ala310Thr) rs199760788
NM_001271620.2(ZNF423):c.964T>C (p.Ser322Pro) rs142835239
NM_001271620.2(ZNF423):c.990G>A (p.Pro330=) rs61747467

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