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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
20
g.33851064G>C
CA408920647
CHMP4B
c.481G>C (p.Glu161Gln)
ClinVar
dbSNP
20
g.33851064G>A
CA114744
CHMP4B
c.481G>A (p.Glu161Lys)
ClinVar
dbSNP
COSMIC
Number of alleles fetched
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