Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.97855197G>TCA12994273FOXE1c.*161G>T (n.*161G>T)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.97855197G>ACA1866643603FOXE1c.*161G>A (n.*161G>A)
dbSNP gnomAD v4
9g.97855197G>CCA1866643604FOXE1c.*161G>C (n.*161G>C)
dbSNP gnomAD v4

Number of alleles fetched