ClinVar Miner

List of variants in gene HNF4A reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_175914.5(HNF4A):c.50-5C>T rs745975 0.17964
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.319+19C>T rs112386711 0.01208
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.1137C>T (p.Asn379=) rs61737145 0.00384
NM_175914.5(HNF4A):c.744C>T (p.Asp248=) rs6031592 0.00257
NM_175914.5(HNF4A):c.84G>A (p.Ala28=) rs41282026 0.00084
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.921C>T (p.Asp307=) rs151168174 0.00039
NM_175914.5(HNF4A):c.1176C>T (p.Asn392=) rs141448616 0.00033
NM_175914.5(HNF4A):c.50-4753G>A rs566155738 0.00016
NM_175914.5(HNF4A):c.670+7C>T rs376544046 0.00005
NM_175914.5(HNF4A):c.50-4665C>T rs774093087 0.00003
NM_175914.5(HNF4A):c.-181G>A rs2146126966
NM_175914.5(HNF4A):c.1185G>A (p.Met395Ile)
NM_175914.5(HNF4A):c.138G>T (p.Thr46=)
NM_175914.5(HNF4A):c.224+2T>G
NM_175914.5(HNF4A):c.225-21A>G
NM_175914.5(HNF4A):c.50-3406A>G
NM_175914.5(HNF4A):c.50-4562G>A
NM_175914.5(HNF4A):c.50-4563G>A
NM_175914.5(HNF4A):c.50-4746G>A
NM_175914.5(HNF4A):c.50-4747C>G
NM_175914.5(HNF4A):c.50-4751_50-4745del rs555295035
NM_175914.5(HNF4A):c.50-4754C>G
NM_175914.5(HNF4A):c.50-4758A>G
NM_175914.5(HNF4A):c.50-4G>A
NM_175914.5(HNF4A):c.670+18C>A rs751211080
NM_175914.5(HNF4A):c.742G>T (p.Asp248Tyr) rs2146445464
NM_175914.5(HNF4A):c.827-6T>C
NM_175914.5(HNF4A):c.869G>A (p.Arg290His) rs1191912908
NM_175914.5(HNF4A):c.881_882delinsCC (p.Gln294Pro)
NM_175914.5(HNF4A):c.911G>A (p.Arg304His)
NM_175914.5(HNF4A):c.937G>A (p.Gly313Arg)
NM_175914.5(HNF4A):c.952C>T (p.Leu318=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.