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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
17
g.41571515G>C
CA115911
KRT9
c.478C>G (p.Leu160Val)
c.-189-33C>G (n.-189-33C>G)
ClinVar
dbSNP
17
g.41571515G>A
CA115914
KRT9
c.478C>T (p.Leu160Phe)
c.-189-33C>T (n.-189-33C>T)
ClinVar
dbSNP
Number of alleles fetched
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