List of variants in gene BRPF1 reported by OMIM

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001003694.2(BRPF1):c.2497C>T (p.Arg833Ter)	rs1057519512	0.00001
NM_001003694.2(BRPF1):c.104dup (p.Tyr35Ter)	rs1057519517
NM_001003694.2(BRPF1):c.1052_1053del (p.Val351fs)	rs886041090
NM_001003694.2(BRPF1):c.1108C>T (p.Pro370Ser)	rs1057519509
NM_001003694.2(BRPF1):c.1165T>C (p.Cys389Arg)	rs1057519515
NM_001003694.2(BRPF1):c.1363C>T (p.Arg455Ter)	rs1057519510
NM_001003694.2(BRPF1):c.2982C>G (p.Tyr994Ter)	rs1057519514
NM_001003694.2(BRPF1):c.3298C>T (p.Arg1100Ter)	rs1057519513
NM_001003694.2(BRPF1):c.362_363del (p.Glu121fs)	rs1057519511
NM_001003694.2(BRPF1):c.567del (p.Asp190fs)	rs1057519516

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.