ClinVar Miner

List of variants in gene F8 reported as uncertain significance

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Total variants: 28
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HGVS dbSNP
NM_000132.3(F8):c.*1166A>G rs984572217
NM_000132.3(F8):c.*1175G>C rs950453657
NM_000132.3(F8):c.*418_*419TC[1] rs1057515825
NM_000132.3(F8):c.*426G>A rs782273756
NM_000132.3(F8):c.*78C>T rs782435894
NM_000132.3(F8):c.*862A>G rs1057515824
NM_000132.3(F8):c.-157A>G rs1057515826
NM_000132.3(F8):c.1301G>T (p.Gly434Val) rs1569559866
NM_000132.3(F8):c.1601T>C (p.Val534Ala) rs1557281261
NM_000132.3(F8):c.244A>G (p.Lys82Glu) rs1283070296
NM_000132.3(F8):c.2947G>A (p.Val983Ile) rs35295375
NM_000132.3(F8):c.3169G>A (p.Glu1057Lys) rs28933673
NM_000132.3(F8):c.359T>C (p.Val120Ala) rs1569560006
NM_000132.3(F8):c.3885C>G (p.Asn1295Lys) rs201393905
NM_000132.3(F8):c.3980C>T (p.Thr1327Met)
NM_000132.3(F8):c.4442T>C (p.Leu1481Pro) rs1800294
NM_000132.3(F8):c.5164G>A (p.Val1722Met)
NM_000132.3(F8):c.5587-98G>A
NM_000132.3(F8):c.599A>G (p.Glu200Gly) rs782158761
NM_000132.3(F8):c.6245G>A (p.Ser2082Asn) rs1569559494
NM_000132.3(F8):c.6623A>G (p.Gln2208Arg) rs782198570
NM_000132.3(F8):c.6724G>A (p.Val2242Met) rs782654096
NM_000132.3(F8):c.6751G>A (p.Val2251Met)
NM_000132.3(F8):c.6871A>G (p.Thr2291Ala) rs139348729
NM_000132.3(F8):c.6901-725T>C
NM_000132.3(F8):c.6991A>T (p.Ser2331Cys) rs1557271047
NM_000132.3(F8):c.788-14T>G
NM_000132.3(F8):c.926C>T (p.Pro309Leu)

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