"CSER _CC_NCGL, University of Washington"[submitter] AND "SERPINC1"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 18038	NM_000488.4(SERPINC1):c.1256C>T (p.Ala419Val)	SERPINC1 (A419V +6 more)	Single nucleotide variant (missense variant)	Hereditary antithrombin deficiency	GUncertain significance
Select item 18023	NM_000488.4(SERPINC1):c.1246G>T (p.Ala416Ser)	SERPINC1 (A416S +6 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 161390	NM_000488.4(SERPINC1):c.886G>C (p.Ala296Pro)	SERPINC1 (A296P +6 more)	Single nucleotide variant (missense variant)	Hereditary antithrombin deficiency	GUncertain significance
Select item 18030	NM_000488.4(SERPINC1):c.482G>A (p.Arg161Gln)	SERPINC1 (R161Q +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary antithrombin deficiency	GPathogenic FDA Recognized database
Select item 18014	NM_000488.4(SERPINC1):c.236G>A (p.Arg79His)	SERPINC1 (R79H +2 more)	Single nucleotide variant (missense variant)	Hereditary antithrombin deficiency	GPathogenic FDA Recognized database
Select item 18011	NM_000488.4(SERPINC1):c.218C>T (p.Pro73Leu)	SERPINC1 (P73L +2 more)	Single nucleotide variant (missense variant)	Hereditary antithrombin deficiency	GPathogenic FDA Recognized database

ClinVar