ClinVar Miner

List of variants in gene F8 reported as benign for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_000132.2:c.*8899A>G
NM_000132.3(F8):c.*1214G>A rs34700571
NM_000132.3(F8):c.*1416G>T rs186338743
NM_000132.3(F8):c.*1672G>A rs1050705
NM_000132.3(F8):c.*29C>T rs5986887
NM_000132.3(F8):c.1010-27G>A rs7058826
NM_000132.3(F8):c.1086G>A (p.Ala362=) rs1800289
NM_000132.3(F8):c.1444-22T>C rs5986899
NM_000132.3(F8):c.1508G>A (p.Arg503His) rs35383156
NM_000132.3(F8):c.1866T>C (p.Leu622=) rs1800290
NM_000132.3(F8):c.266-19G>A rs28370201
NM_000132.3(F8):c.2947G>A (p.Val983Ile) rs35295375
NM_000132.3(F8):c.2994T>G (p.His998Gln) rs149853218
NM_000132.3(F8):c.3780C>G (p.Asp1260Glu) rs1800291
NM_000132.3(F8):c.3864A>C (p.Ser1288=) rs1800292
NM_000132.3(F8):c.389-9C>T rs35621875
NM_000132.3(F8):c.4500G>A (p.Pro1500=) rs33921347
NM_000132.3(F8):c.5493C>G (p.Thr1831=) rs1603432997
NM_000132.3(F8):c.6724G>A (p.Val2242Met) rs782654096
NM_000132.3(F8):c.6769A>G (p.Met2257Val) rs1800297
NM_000132.3(F8):c.6849C>T (p.Ser2283=) rs1319284046
NM_000132.4(F8):c.*1001C>T
NM_000132.4(F8):c.3236G>A (p.Arg1079Lys)
NM_000132.4(F8):c.4467C>G (p.Val1489=)
NM_000132.4(F8):c.989A>G (p.His330Arg)

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