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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
13
g.32338040del
CA018575
BRCA2
c.3685del (p.Val1229PhefsTer10)
c.3316del (p.Val1106PhefsTer10)
n.3685del
ClinVar
dbSNP
13
g.32338040G=
CA2082819630
BRCA2
c.3685G= (p.Val1229=)
c.3316G= (p.Val1106=)
n.3685G=
dbSNP
dbSNP
Number of alleles fetched
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