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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
13
g.32339214T>G
CA020929
BRCA2
c.4859T>G (p.Leu1620Ter)
c.4490T>G (p.Leu1497Ter)
n.4859T>G
ClinVar
dbSNP
gnomAD v2
gnomAD v4
13
g.32339214T>A
CA387783418
BRCA2
c.4859T>A (p.Leu1620Ter)
c.4490T>A (p.Leu1497Ter)
n.4859T>A
dbSNP
Number of alleles fetched
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