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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
X
g.154904026G>A
CA255024
F8
c.5878C>T (p.Arg1960Ter)
c.5773C>T (p.Arg1925Ter)
ClinVar
dbSNP
X
g.154904026G>T
CA10567927
F8
c.5878C>A (p.Arg1960=)
c.5773C>A (p.Arg1925=)
dbSNP
ExAC
gnomAD v2
gnomAD v4
Number of alleles fetched
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