List of variants in gene PLG studied for Plasminogen deficiency, type I

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

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP
NM_000301.3(PLG):c.1217C>A (p.Pro406Gln)
NM_000301.3(PLG):c.1435G>T (p.Glu479Ter)	rs121918032
NM_000301.3(PLG):c.1469G>A (p.Arg490Gln)	rs140537724
NM_000301.3(PLG):c.1848G>A (p.Trp616Ter)	rs121918031
NM_000301.3(PLG):c.1858G>A (p.Ala620Thr)	rs121918027
NM_000301.3(PLG):c.2125+1del	rs606231210
NM_000301.3(PLG):c.2278A>G (p.Ser760Gly)
NM_000301.3(PLG):c.687_689GAA[2] (p.Lys231del)	rs121918034
NM_000301.3(PLG):c.704G>A (p.Arg235His)	rs121918030
NM_000301.3(PLG):c.950+4A>G
NM_001168338.1(PLG):c.112A>G (p.Lys38Glu)	rs73015965

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.