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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
19
g.15544007C>T
CA9269801
CYP4F22
c.976C>T (p.Arg326Ter)
ClinVar
dbSNP
ExAC
gnomAD v2
gnomAD v3
gnomAD v4
COSMIC
19
g.15544007C>G
CA404538833
CYP4F22
c.976C>G (p.Arg326Gly)
dbSNP
gnomAD v3
gnomAD v4
Number of alleles fetched
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