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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
X
g.111410223C>A
CA121596
DCX
c.176G>T (p.Arg59Leu)
c.419G>T (p.Arg140Leu)
c.394G>T
n.416G>T
ClinVar
dbSNP
X
g.111410223C>T
CA171866
DCX
c.176G>A (p.Arg59His)
c.419G>A (p.Arg140His)
c.394G>A
n.416G>A
ClinVar
dbSNP
COSMIC
Number of alleles fetched
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