ClinVar Miner

List of variants in gene F8 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 17
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HGVS dbSNP
NM_000132.3(F8):c.102C>T (p.Asp34=) rs1800283
NM_000132.3(F8):c.1064G>A (p.Arg355Gln)
NM_000132.3(F8):c.1508G>A (p.Arg503His) rs35383156
NM_000132.3(F8):c.2383A>G (p.Arg795Gly) rs2228152
NM_000132.3(F8):c.2535C>A (p.Asp845Glu) rs200316756
NM_000132.3(F8):c.2994T>G (p.His998Gln) rs149853218
NM_000132.3(F8):c.3885C>G (p.Asn1295Lys) rs201393905
NM_000132.3(F8):c.389-9C>T rs35621875
NM_000132.3(F8):c.6957G>A (p.Pro2319=) rs200902529
NM_000132.3(F8):c.748A>G (p.Met250Val) rs781943293
NM_000132.4(F8):c.*1379A>G
NM_000132.4(F8):c.*30G>A
NM_000132.4(F8):c.*992A>G
NM_000132.4(F8):c.2212T>G (p.Tyr738Asp)
NM_000132.4(F8):c.2217G>A (p.Glu739=)
NM_000132.4(F8):c.3981G>A (p.Thr1327=)
NM_000132.4(F8):c.4679C>G (p.Pro1560Arg)

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