List of variants reported as uncertain significance for Thrombophilia due to protein C deficiency, autosomal recessive; Thrombophilia due to protein C deficiency, autosomal dominant

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000312.4(PROC):c.-21-5C>T	rs41269833	0.00172
NM_000312.4(PROC):c.*146T>C	rs140461934	0.00158
NM_000312.4(PROC):c.1234G>A (p.Gly412Ser)	rs139741458	0.00011
NM_000312.4(PROC):c.322C>A (p.His108Asn)	rs200234655	0.00007
NM_000312.4(PROC):c.52G>A (p.Gly18Ser)	rs146793243	0.00006
NM_000312.4(PROC):c.113G>A (p.Arg38Gln)	rs773107370	0.00004
NM_000312.4(PROC):c.534A>G (p.Ala178=)	rs368367611	0.00004
NM_000312.4(PROC):c.386G>A (p.Arg129His)	rs746190838	0.00003
NM_000312.4(PROC):c.160A>T (p.Ser54Cys)	rs376049280	0.00002
NM_000312.4(PROC):c.1241G>C (p.Trp414Ser)	rs768759265	0.00001
NM_000312.4(PROC):c.1333A>C (p.Ile445Leu)	rs200012319	0.00001
NM_000312.4(PROC):c.340G>C (p.Gly114Arg)	rs374476971	0.00001
NM_000312.4(PROC):c.372C>G (p.Ser124Arg)	rs939496684	0.00001
NM_000312.4(PROC):c.881G>A (p.Ser294Asn)	rs200721675	0.00001
NM_000312.4(PROC):c.1181G>A (p.Arg394Gln)
NM_000312.4(PROC):c.263-28T>G	rs2104952137
NM_000312.4(PROC):c.505G>T (p.Gly169Trp)	rs989908811

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