"Genome-Nilou Lab"[submitter] AND "PLG"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1242787	NM_000301.5(PLG):c.330C>T (p.Asn110=)	PLG	Single nucleotide variant (synonymous variant)	Plasminogen deficiency, type I +2 more	GBenign
Select item 1175116	NM_000301.5(PLG):c.771T>C (p.Cys257=)	PLG	Single nucleotide variant (synonymous variant)	Plasminogen deficiency, type I +2 more	GBenign
Select item 1174797	NM_000301.5(PLG):c.942C>T (p.Phe314=)	PLG	Single nucleotide variant (synonymous variant)	Plasminogen deficiency, type I +2 more	GBenign
Select item 1174642	NM_000301.5(PLG):c.950+14G>A	PLG	Single nucleotide variant (intron variant)	Angioedema, hereditary, 4 +2 more	GBenign
Select item 1263884	NM_000301.5(PLG):c.1878-17G>A	PLG	Single nucleotide variant (intron variant)	Plasminogen deficiency, type I +2 more	GBenign
Select item 1241596	NM_000301.5(PLG):c.2286T>G (p.Gly762=)	PLG	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 1247506	NM_000301.5(PLG):c.*45A>G	PLG	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign

ClinVar