List of variants in gene POU3F4 reported as uncertain significance for Inborn genetic diseases

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000307.5(POU3F4):c.359C>A (p.Pro120Gln)	rs765593474	0.00023
NM_000307.5(POU3F4):c.506C>T (p.Pro169Leu)	rs200696740	0.00013
NM_000307.5(POU3F4):c.418A>C (p.Thr140Pro)	rs186010225	0.00010
NM_000307.5(POU3F4):c.305C>G (p.Ala102Gly)	rs772013350	0.00003
NM_000307.5(POU3F4):c.353C>T (p.Pro118Leu)	rs760582733	0.00003
NM_000307.5(POU3F4):c.119G>C (p.Ser40Thr)	rs988801509	0.00001
NM_000307.5(POU3F4):c.301G>A (p.Val101Ile)	rs375260287	0.00001
NM_000307.5(POU3F4):c.167A>C (p.His56Pro)
NM_000307.5(POU3F4):c.17C>G (p.Ser6Trp)	rs1219469566
NM_000307.5(POU3F4):c.280A>G (p.Ile94Val)	rs748726844
NM_000307.5(POU3F4):c.370A>G (p.Ile124Val)	rs2520215978
NM_000307.5(POU3F4):c.547C>G (p.His183Asp)

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.