Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.1610780T>ACA3614742FOXC1c.335T>A (p.Phe112Tyr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.1610780T>CCA119636FOXC1c.335T>C (p.Phe112Ser)
 ClinVar dbSNP
6g.1610780T=CA1605822499FOXC1c.335T= (p.Phe112=)
 dbSNP

Number of alleles fetched