List of variants in gene GRN reported by Institute Of Human Genetics Munich, Klinikum Rechts Der Isar, Tu München

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002087.4(GRN):c.103G>A (p.Gly35Arg)	rs533451404	0.00002
NM_002087.4(GRN):c.1252C>T (p.Arg418Ter)	rs63751180
NM_002087.4(GRN):c.146G>A (p.Trp49Ter)	rs1598362746
NM_002087.4(GRN):c.264G>A (p.Glu88=)	rs63751166
NM_002087.4(GRN):c.328C>T (p.Arg110Ter)	rs63750411
NM_002087.4(GRN):c.349+1G>C	rs1598363083
NM_002087.4(GRN):c.424dup (p.Met142fs)	rs1598363490
NM_002087.4(GRN):c.675_676del (p.Ser226fs)	rs63751085
NM_002087.4(GRN):c.759_760del (p.Cys253_Asp254delinsTer)	rs63751035
NM_002087.4(GRN):c.882T>G (p.Tyr294Ter)	rs794729670
NM_002087.4(GRN):c.918C>A (p.Cys306Ter)	rs1598364782

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.