Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.28768479C>ACA235611FOXG1c.1200C>A (p.Tyr400Ter)
ClinVar dbSNP
14g.28768479C>GCA123557FOXG1c.1200C>G (p.Tyr400Ter)
ClinVar dbSNP
14g.28768479C>TCA7140671FOXG1c.1200C>T (p.Tyr400=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched