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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
6
g.1610901G>A
CA10603005
FOXC1
c.456G>A (p.Trp152Ter)
ClinVar
dbSNP
6
g.1610901G>T
CA362558863
FOXC1
c.456G>T (p.Trp152Cys)
ClinVar
dbSNP
Number of alleles fetched
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