Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32362593T>ACA16614217BRCA2c.7876T>A (p.Trp2626Arg)
c.7507T>A (p.Trp2503Arg)
c.343T>A (p.Trp115Arg)
c.7884T>A (p.Asp2628Glu)
c.441T>A
n.7884T>A
c.7780T>A (p.Trp2594Arg)
ClinVar dbSNP
13g.32362593T>CCA387747100BRCA2c.7876T>C (p.Trp2626Arg)
c.7507T>C (p.Trp2503Arg)
c.343T>C (p.Trp115Arg)
c.7884T>C (p.Asp2628=)
c.441T>C
n.7884T>C
c.7780T>C (p.Trp2594Arg)
ClinVar dbSNP

Number of alleles fetched