"Ambry Genetics"[submitter] AND "SERPINC1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2363552	NM_000488.4(SERPINC1):c.1061G>A (p.Arg354His)	SERPINC1 (R282H +6 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2178499	NM_000488.4(SERPINC1):c.1051C>T (p.His351Tyr)	SERPINC1 (H351Y +6 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 3160464	NM_000488.4(SERPINC1):c.848T>C (p.Met283Thr)	SERPINC1 (M211T +6 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3160463	NM_000488.4(SERPINC1):c.433G>A (p.Glu145Lys)	SERPINC1 (E145K +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2267274	NM_000488.4(SERPINC1):c.223G>A (p.Ala75Thr)	SERPINC1 (A102T +2 more)	Single nucleotide variant (missense variant)	Hereditary antithrombin deficiency	GUncertain significance FDA Recognized database
Select item 2295171	NM_000488.4(SERPINC1):c.17T>C (p.Ile6Thr)	SERPINC1 (I6T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3317617	NM_000488.4(SERPINC1):c.13G>A (p.Val5Met)	SERPINC1 (V5M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar