Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.1610780T>CCA119636FOXC1n.335T>C (p.Phe112Ser)
c.335T>C (p.Phe112Ser)
ClinVar dbSNP
6g.1610780T>ACA3614742FOXC1n.335T>A (p.Phe112Tyr)
c.335T>A (p.Phe112Tyr)
dbSNP ExAC gnomAD

Number of alleles fetched