Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.28767790G>TCA16042885FOXG1c.511G>T (p.Glu171Ter)
ClinVar dbSNP gnomAD v4
14g.28767790G=CA2125999668FOXG1c.511G= (p.Glu171=)
dbSNP

Number of alleles fetched