List of variants studied for protein S deficiency by CSER _CC_NCGL, University of Washington

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000313.4(PROS1):c.1528G>A (p.Val510Met)	rs138925964	0.00331
NM_000313.4(PROS1):c.698G>A (p.Arg233Lys)	rs41267007	0.00202
NM_000313.4(PROS1):c.1095T>G (p.Asn365Lys)	rs199469491	0.00155
NM_000313.4(PROS1):c.1762A>G (p.Thr588Ala)	rs142846443	0.00043
NM_000313.4(PROS1):c.284G>A (p.Gly95Glu)	rs144526169	0.00040
NM_000313.4(PROS1):c.431C>A (p.Thr144Asn)	rs146366248	0.00029
NM_000313.4(PROS1):c.1747A>C (p.Asn583His)	rs139479630	0.00014
NM_000313.4(PROS1):c.1331C>T (p.Pro444Leu)	rs369244777	0.00009
NM_000313.4(PROS1):c.1594A>G (p.Thr532Ala)	rs371028997	0.00001
NM_000313.4(PROS1):c.946C>T (p.Arg316Cys)	rs373983977	0.00001
NM_000313.4(PROS1):c.1907A>G (p.Tyr636Cys)	rs368173480
NM_000313.4(PROS1):c.676T>A (p.Cys226Ser)	rs370855515
NM_000313.4(PROS1):c.728-1G>A	rs368074804

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