Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107702023T>CCA368843803SLC26A4c.2000T>C (p.Phe667Ser)
c.711T>C
n.287T>C
c.1922T>C (p.Phe641Ser)
ClinVar dbSNP gnomAD v4
7g.107702023T>GCA253303SLC26A4c.2000T>G (p.Phe667Cys)
c.711T>G
n.287T>G
c.1922T>G (p.Phe641Cys)
ClinVar dbSNP

Number of alleles fetched