ClinVar Miner

List of variants in gene HNF4A reported as likely benign by Labcorp Genetics (formerly Invitae), Labcorp

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Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_175914.5(HNF4A):c.426+6G>A rs182980547 0.00070
NM_175914.5(HNF4A):c.726G>A (p.Val242=) rs145280017 0.00041
NM_175914.5(HNF4A):c.921C>T (p.Asp307=) rs151168174 0.00039
NM_175914.5(HNF4A):c.1176C>T (p.Asn392=) rs141448616 0.00033
NM_175914.5(HNF4A):c.582+20G>C rs370794722 0.00024
NM_175914.5(HNF4A):c.576C>T (p.Asp192=) rs759574096 0.00019
NM_175914.5(HNF4A):c.50-4753G>A rs566155738 0.00016
NM_175914.5(HNF4A):c.582+12C>T rs372596032 0.00016
NM_175914.5(HNF4A):c.427-5C>T rs374703326 0.00009
NM_175914.5(HNF4A):c.1064-19C>T rs202202465 0.00007
NM_175914.5(HNF4A):c.225-8C>T rs759922116 0.00006
NM_175914.5(HNF4A):c.381G>A (p.Leu127=) rs193922473 0.00006
NM_175914.5(HNF4A):c.427-16C>T rs535994220 0.00006
NM_175914.5(HNF4A):c.670+7C>T rs376544046 0.00005
NM_175914.5(HNF4A):c.1026C>T (p.Ala342=) rs751892618 0.00004
NM_175914.5(HNF4A):c.1284G>A (p.Pro428=) rs377052026 0.00004
NM_175914.5(HNF4A):c.1017C>T (p.Phe339=) rs142268325 0.00003
NM_175914.5(HNF4A):c.396G>A (p.Ala132=) rs370329321 0.00003
NM_175914.5(HNF4A):c.657C>T (p.Asp219=) rs376586083 0.00003
NM_175914.5(HNF4A):c.319+10G>A rs375708199 0.00002
NM_175914.5(HNF4A):c.123C>T (p.Cys41=) rs147552575 0.00001
NM_175914.5(HNF4A):c.126G>C (p.Gly42=) rs781364773 0.00001
NM_175914.5(HNF4A):c.1302C>T (p.Ile434=) rs199884828 0.00001
NM_175914.5(HNF4A):c.321C>T (p.Ala107=) rs138290205 0.00001
NM_175914.5(HNF4A):c.489A>G (p.Ala163=) rs1568731613 0.00001
NM_175914.5(HNF4A):c.105C>T (p.Ser35=)
NM_175914.5(HNF4A):c.1167C>T (p.His389=)
NM_175914.5(HNF4A):c.12G>C (p.Val4=)
NM_175914.5(HNF4A):c.150C>T (p.Tyr50=)
NM_175914.5(HNF4A):c.156C>T (p.Ala52=)
NM_175914.5(HNF4A):c.168C>T (p.Asp56=)
NM_175914.5(HNF4A):c.228T>C (p.Phe76=)
NM_175914.5(HNF4A):c.282G>A (p.Arg94=) rs1463516865
NM_175914.5(HNF4A):c.333G>A (p.Glu111=)
NM_175914.5(HNF4A):c.372C>T (p.Asp124=)
NM_175914.5(HNF4A):c.405G>A (p.Gln135=)
NM_175914.5(HNF4A):c.426+7G>C rs1600723028
NM_175914.5(HNF4A):c.427-5C>G
NM_175914.5(HNF4A):c.474G>A (p.Lys158=)
NM_175914.5(HNF4A):c.49+15G>A
NM_175914.5(HNF4A):c.50-4749G>A
NM_175914.5(HNF4A):c.50-4751A>G
NM_175914.5(HNF4A):c.528C>T (p.Leu176=)
NM_175914.5(HNF4A):c.561C>T (p.Cys187=)
NM_175914.5(HNF4A):c.582+13G>A rs201219009
NM_175914.5(HNF4A):c.582+20G>A
NM_175914.5(HNF4A):c.582+9G>A
NM_175914.5(HNF4A):c.583-7C>T
NM_175914.5(HNF4A):c.642C>T (p.Ser214=)
NM_175914.5(HNF4A):c.661C>T (p.Leu221=)
NM_175914.5(HNF4A):c.670+14C>G
NM_175914.5(HNF4A):c.670+8G>A
NM_175914.5(HNF4A):c.671-13C>T
NM_175914.5(HNF4A):c.671-18C>G
NM_175914.5(HNF4A):c.672C>A (p.Gly224=)
NM_175914.5(HNF4A):c.726G>C (p.Val242=) rs145280017
NM_175914.5(HNF4A):c.780T>C (p.Asp260=)
NM_175914.5(HNF4A):c.7A>C (p.Ser3Arg)
NM_175914.5(HNF4A):c.912C>A (p.Arg304=) rs760811566

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