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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
11
g.22625484G>C
CA253847
FANCF
c.327C>G (p.Tyr109Ter)
ClinVar
dbSNP
11
g.22625484G>A
CA473533715
FANCF
c.327C>T (p.Tyr109=)
dbSNP
gnomAD v2
gnomAD v3
gnomAD v4
Number of alleles fetched
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