Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.49258503C>TCA255872FOXP3c.3G>A (p.Met1Ile)
c.17-59G>A (n.17-59G>A)
c.327G>A (p.Met109Ile)
c.54G>A (p.Met18Ile)
ClinVar dbSNP gnomAD v4
Xg.49258503C=CA2428553628FOXP3c.3G= (p.Met1=)
c.17-59G= (n.17-59G=)
c.327G= (p.Met109=)
c.54G= (p.Met18=)
dbSNP

Number of alleles fetched