Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.49256855G>ACA152905FOXP3c.438C>T (p.Ser146=)
c.543C>T (p.Ser181=)
c.612C>T (p.Ser204=)
c.396C>T (p.Ser132=)
c.393C>T (p.Ser131=)
c.762C>T (p.Ser254=)
c.561C>T (p.Ser187=)
c.798C>T (p.Ser266=)
c.489C>T (p.Ser163=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.49256855G=CA2428553143FOXP3c.438C= (p.Ser146=)
c.543C= (p.Ser181=)
c.612C= (p.Ser204=)
c.396C= (p.Ser132=)
c.393C= (p.Ser131=)
c.762C= (p.Ser254=)
c.561C= (p.Ser187=)
c.798C= (p.Ser266=)
c.489C= (p.Ser163=)
dbSNP

Number of alleles fetched