List of variants in gene PRMT7 reported as pathogenic for syndromic intellectual disability

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: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_019023.5(PRMT7):c.1056-1G>T	rs201824659	0.00008
NM_019023.5(PRMT7):c.95G>C (p.Arg32Thr)	rs149170494	0.00003
NM_019023.5(PRMT7):c.1159A>G (p.Arg387Gly)	rs762515973	0.00001
NM_019023.5(PRMT7):c.1480T>C (p.Trp494Arg)	rs751670999	0.00001
NC_000016.9:g.68345747_68361056del
NM_019023.5(PRMT7):c.1074_1075del (p.Arg358fs)	rs763953657
NM_019023.5(PRMT7):c.1097G>A (p.Cys366Tyr)	rs2151827144
NM_019023.5(PRMT7):c.1168C>T (p.Arg390Ter)
NM_019023.5(PRMT7):c.1173C>G (p.Tyr391Ter)
NM_019023.5(PRMT7):c.1239_1246dup (p.Val416fs)	rs1567721991
NM_019023.5(PRMT7):c.1276-1G>A	rs886039897
NM_019023.5(PRMT7):c.1678del (p.Glu560fs)
NM_019023.5(PRMT7):c.431_432del (p.Glu144fs)	rs1567690011
NM_019023.5(PRMT7):c.477T>A (p.Tyr159Ter)
NM_019023.5(PRMT7):c.622del (p.Gln208fs)	rs2151732301
NM_019023.5(PRMT7):c.967C>T (p.Gln323Ter)
NM_019023.5(PRMT7):c.98C>A (p.Ser33Ter)	rs2151436426

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.