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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
7
g.107702023T>C
CA368843803
SLC26A4
c.2000T>C (p.Phe667Ser)
c.711T>C
n.287T>C
c.1922T>C (p.Phe641Ser)
ClinVar
dbSNP
gnomAD v4
7
g.107702023T>G
CA253303
SLC26A4
c.2000T>G (p.Phe667Cys)
c.711T>G
n.287T>G
c.1922T>G (p.Phe641Cys)
ClinVar
dbSNP
Number of alleles fetched
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