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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
13
g.32338431del
CA019472
BRCA2
c.4076del (p.Thr1359MetfsTer15)
c.3707del (p.Thr1236MetfsTer15)
n.4076del
ClinVar
dbSNP
13
g.32338431C=
CA2082823621
BRCA2
c.4076C= (p.Thr1359=)
c.3707C= (p.Thr1236=)
n.4076C=
dbSNP
dbSNP
Number of alleles fetched
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