List of variants in gene HSF4 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001374675.1(HSF4):c.1414A>G (p.Ile472Val)	rs201011907	0.00303
NM_001374675.1(HSF4):c.636G>T (p.Met212Ile)	rs199742128	0.00196
NM_001374675.1(HSF4):c.925C>G (p.Leu309Val)	rs201430635	0.00115
NM_001374675.1(HSF4):c.63C>A (p.Leu21=)	rs372135101	0.00041
NM_001374675.1(HSF4):c.680C>A (p.Thr227Asn)	rs200708134	0.00025
NM_001374675.1(HSF4):c.510G>A (p.Glu170=)	rs372473149	0.00008
NM_001374675.1(HSF4):c.806C>T (p.Ser269Phe)	rs760449871	0.00002
NM_001374675.1(HSF4):c.1341C>G (p.Leu447=)	rs35750776
NM_001374675.1(HSF4):c.293A>T (p.His98Leu)	rs1264444474

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.