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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
14
g.28767790G>T
CA16042885
FOXG1
c.511G>T (p.Glu171Ter)
ClinVar
dbSNP
gnomAD v4
14
g.28767790G=
CA2125999668
FOXG1
c.511G= (p.Glu171=)
dbSNP
Number of alleles fetched
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