Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32336594G>C | CA387770810 | BRCA2 | c.2239G>C (p.Glu747Gln) c.1870G>C (p.Glu624Gln) n.2239G>C | ClinVar dbSNP |
13 | g.32336594G>T | CA10583079 | BRCA2 | c.2239G>T (p.Glu747Ter) c.1870G>T (p.Glu624Ter) n.2239G>T | ClinVar dbSNP |
13 | g.32336594G>A | CA16607460 | BRCA2 | c.2239G>A (p.Glu747Lys) c.1870G>A (p.Glu624Lys) n.2239G>A | ClinVar dbSNP |