Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32355228A>G | CA387741629 | BRCA2 | c.7375A>G (p.Lys2459Glu) c.7006A>G (p.Lys2336Glu) n.7375A>G c.7279A>G (p.Lys2427Glu) | ClinVar dbSNP |
13 | g.32355228A>C | CA387741625 | BRCA2 | c.7375A>C (p.Lys2459Gln) c.7006A>C (p.Lys2336Gln) n.7375A>C c.7279A>C (p.Lys2427Gln) | ClinVar dbSNP |
13 | g.32355228A>T | CA025046 | BRCA2 | c.7375A>T (p.Lys2459Ter) c.7006A>T (p.Lys2336Ter) n.7375A>T c.7279A>T (p.Lys2427Ter) | ClinVar dbSNP |
13 | g.32355228A= | CA2082811366 | BRCA2 | c.7375A= (p.Lys2459=) c.7006A= (p.Lys2336=) n.7375A= c.7279A= (p.Lys2427=) | dbSNP |