ClinVar Miner

List of variants in gene HNF4A reported as uncertain significance by GeneDx

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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_175914.5(HNF4A):c.724G>A (p.Val242Met) rs139779712 0.00019
NM_175914.5(HNF4A):c.464G>A (p.Arg155Gln) rs142883089 0.00009
NM_175914.5(HNF4A):c.340C>T (p.Arg114Trp) rs137853336 0.00006
NM_175914.5(HNF4A):c.361A>G (p.Ser121Gly) rs193922472 0.00006
NM_175914.5(HNF4A):c.1138G>A (p.Val380Ile) rs137853337 0.00001
NM_175914.5(HNF4A):c.232C>T (p.Arg78Trp) rs780813696 0.00001
NM_175914.5(HNF4A):c.587C>A (p.Ala196Asp) rs1032164393 0.00001
NM_175914.5(HNF4A):c.625G>A (p.Gly209Arg) rs1469544671 0.00001
NM_175914.5(HNF4A):c.733C>T (p.Arg245Cys) rs1290868034 0.00001
NM_175914.5(HNF4A):c.76C>A (p.Leu26Ile) rs753285226 0.00001
NM_175914.5(HNF4A):c.862C>T (p.Arg288Trp) rs768263630 0.00001
NM_175914.5(HNF4A):c.910C>T (p.Arg304Cys) rs1486917678 0.00001
NM_175914.5(HNF4A):c.925C>T (p.Arg309Cys) rs193922479 0.00001
NM_175914.5(HNF4A):c.926G>A (p.Arg309His) rs369429452 0.00001
NC_000020.11:g.44355626_44355638del rs2146126980
NC_000020.11:g.44355673A>G rs2146127040
NM_175914.5(HNF4A):c.1035C>T (p.Asp345=)
NM_175914.5(HNF4A):c.119T>A (p.Ile40Asn) rs2146367925
NM_175914.5(HNF4A):c.1288G>A (p.Ala430Thr) rs1281910350
NM_175914.5(HNF4A):c.128A>T (p.Asp43Val) rs1600707598
NM_175914.5(HNF4A):c.195C>A (p.Ser65Arg) rs1008906897
NM_175914.5(HNF4A):c.200G>A (p.Arg67Gln) rs1555813319
NM_175914.5(HNF4A):c.239G>A (p.Cys80Tyr) rs2146375487
NM_175914.5(HNF4A):c.2T>C (p.Met1Thr) rs1229650809
NM_175914.5(HNF4A):c.319G>A (p.Ala107Thr) rs2063517684
NM_175914.5(HNF4A):c.577G>T (p.Asp193Tyr)
NM_175914.5(HNF4A):c.725T>G (p.Val242Gly)
NM_175914.5(HNF4A):c.731T>C (p.Ile244Thr)
NM_175914.5(HNF4A):c.733C>A (p.Arg245Ser) rs1290868034
NM_175914.5(HNF4A):c.740T>C (p.Leu247Pro) rs1555816654
NM_175914.5(HNF4A):c.745G>A (p.Glu249Lys)
NM_175914.5(HNF4A):c.931C>T (p.Arg311Cys) rs193922480
NM_175914.5(HNF4A):c.932G>A (p.Arg311His) rs1375557127

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