ClinVar Miner

List of variants in gene HNF4A reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_175914.5(HNF4A):c.50-230A>G rs2868095 0.68049
NM_175914.5(HNF4A):c.224+266C>T rs3212183 0.58030
NM_175914.5(HNF4A):c.1217-67C>G rs3746575 0.56796
NM_175914.5(HNF4A):c.827-88T>C rs2273618 0.56736
NM_175914.5(HNF4A):c.670+141A>G rs6103731 0.55192
NM_175914.5(HNF4A):c.1217-145T>C rs3746574 0.46132
NM_175914.5(HNF4A):c.50-38T>C rs736824 0.44632
NM_175914.5(HNF4A):c.319+2667T>C rs3212191 0.28328
NM_175914.5(HNF4A):c.*1132C>T rs6130615 0.24797
NM_175914.5(HNF4A):c.427-197A>C rs11574739 0.19545
NM_175914.5(HNF4A):c.427-52G>A rs3212195 0.19516
NM_175914.5(HNF4A):c.320-204C>G rs13041396 0.19053
NM_175914.5(HNF4A):c.426+140C>G rs11574738 0.19031
NM_175914.5(HNF4A):c.225-278A>G rs55934816 0.18088
NM_175914.5(HNF4A):c.50-5C>T rs745975 0.17964
NM_175914.5(HNF4A):c.427-96C>G rs3212194 0.15252
NM_175914.5(HNF4A):c.50-185C>G rs3212180 0.13745
NM_175914.5(HNF4A):c.*392T>G rs11086926 0.13032
NM_175914.5(HNF4A):c.225-241C>T rs6093976 0.12430
NM_175914.5(HNF4A):c.50-226C>T rs3212179 0.11154
NM_175914.5(HNF4A):c.50-4263G>A rs2071197 0.10256
NM_175914.5(HNF4A):c.670+196G>A rs11086925 0.07736
NM_175914.5(HNF4A):c.1217-151A>C rs74173201 0.07406
NM_175914.5(HNF4A):c.*305A>G rs56343153 0.04078
NM_175914.5(HNF4A):c.*242T>C rs41282030 0.04068
NM_175914.5(HNF4A):c.50-4538G>A rs113725562 0.03716
NM_175914.5(HNF4A):c.135C>T (p.Ala45=) rs736823 0.03705
NM_175914.5(HNF4A):c.350C>T (p.Thr117Ile) rs1800961 0.02469
NM_175914.5(HNF4A):c.*700T>C rs114764820 0.02223
NM_175914.5(HNF4A):c.50-5034T>C rs112202184 0.02018
NM_175914.5(HNF4A):c.50-4387A>C rs10427469 0.01810
NM_175914.5(HNF4A):c.319+19C>T rs112386711 0.01208
NM_175914.5(HNF4A):c.*155G>A rs41280258 0.01170
NM_175914.5(HNF4A):c.*3086C>T rs551080524 0.00706
NM_175914.5(HNF4A):c.393T>C (p.Asn131=) rs113308087 0.00598
NM_175914.5(HNF4A):c.669A>G (p.Leu223=) rs139591750 0.00425
NM_175914.5(HNF4A):c.583-27G>A rs113495257 0.00408
NM_175914.5(HNF4A):c.1137C>T (p.Asn379=) rs61737145 0.00384
NM_175914.5(HNF4A):c.696C>T (p.His232=) rs150078978 0.00365
NM_175914.5(HNF4A):c.*1127T>C rs757386171 0.00337
NM_175914.5(HNF4A):c.744C>T (p.Asp248=) rs6031592 0.00257
NM_175914.5(HNF4A):c.*1783G>T rs564110189 0.00161
NM_175914.5(HNF4A):c.84G>A (p.Ala28=) rs41282026 0.00084
NM_175914.5(HNF4A):c.426+6G>A rs182980547 0.00070
NM_175914.5(HNF4A):c.1032T>A (p.Ile344=) rs145880201 0.00062
NM_175914.5(HNF4A):c.1321A>G (p.Ile441Val) rs147638455 0.00061
NM_175914.5(HNF4A):c.999C>T (p.Ile333=) rs150247632 0.00045
NM_175914.5(HNF4A):c.138G>A (p.Thr46=) rs145845882 0.00043
NM_175914.5(HNF4A):c.1176C>T (p.Asn392=) rs141448616 0.00033
NM_175914.5(HNF4A):c.439G>A (p.Val147Ile) rs142204928 0.00025
NM_175914.5(HNF4A):c.427-4G>A rs146751799 0.00021
NM_175914.5(HNF4A):c.576C>T (p.Asp192=) rs759574096 0.00019
NM_175914.5(HNF4A):c.408G>A (p.Ala136=) rs374298096 0.00009
NM_175914.5(HNF4A):c.427-20C>T rs184217112 0.00008
NM_175914.5(HNF4A):c.624C>T (p.Leu208=) rs759084238 0.00006
NM_175914.5(HNF4A):c.1017C>T (p.Phe339=) rs142268325 0.00003
NM_175914.5(HNF4A):c.924G>T (p.Ser308=) rs140146223 0.00003
NM_175914.5(HNF4A):c.123C>T (p.Cys41=) rs147552575 0.00001
NM_175914.5(HNF4A):c.1243C>T (p.Pro415Ser) rs150776703 0.00001
NM_175914.5(HNF4A):c.369G>A (p.Glu123=) rs772959288 0.00001
NM_175914.5(HNF4A):c.582+4A>G rs376287515 0.00001
NM_175914.5(HNF4A):c.81C>T (p.Asn27=) rs570058788 0.00001
NM_175914.5(HNF4A):c.*1291TCCTCCCT[1] rs3834658
NM_175914.5(HNF4A):c.*906A>C rs3212210
NM_175914.5(HNF4A):c.*906A>T rs3212210
NM_175914.5(HNF4A):c.*937_*955del rs72137187
NM_175914.5(HNF4A):c.224+17dup rs371937621
NM_175914.5(HNF4A):c.224+288G>C rs3212184
NM_175914.5(HNF4A):c.319+283TG[18] rs35406830
NM_175914.5(HNF4A):c.319+283TG[19] rs35406830
NM_175914.5(HNF4A):c.319+283TG[20] rs35406830
NM_175914.5(HNF4A):c.319+283TG[21] rs35406830
NM_175914.5(HNF4A):c.50-4746G>A
NM_175914.5(HNF4A):c.50-4751_50-4745del rs555295035
NM_175914.5(HNF4A):c.826+169A>G rs3212201

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