| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.102208237C>A | CA345622 | RRM2B | c.952G>T (p.Glu318Ter) n.339G>T c.796G>T (p.Glu266Ter) c.316G>T (p.Glu106Ter) c.97G>T (p.Glu33Ter) c.1121G>T c.285G>T (n.285G>T) c.790G>T (p.Glu264Ter) c.1168G>T (p.Glu390Ter) | ClinVar dbSNP |
| 8 | g.102208237C= | CA1806674685 | RRM2B | c.952G= (p.Glu318=) n.339G= c.796G= (p.Glu266=) c.316G= (p.Glu106=) c.97G= (p.Glu33=) c.1121G= c.285G= (n.285G=) c.790G= (p.Glu264=) c.1168G= (p.Glu390=) | dbSNP |