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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
13
g.32339400del
CA021174
BRCA2
c.5045del (p.Ser1682IlefsTer24)
c.4676del (p.Ser1559IlefsTer24)
n.5045del
ClinVar
dbSNP
13
g.32339400G=
CA2082818383
BRCA2
c.5045G= (p.Ser1682=)
c.4676G= (p.Ser1559=)
n.5045G=
dbSNP
dbSNP
Number of alleles fetched
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