| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.95107082C>T | CA16041337 | AOPEP,FANCC | n.410+26302C>T n.2332G>A c.1517G>A (p.Trp506Ter) c.1662G>A (n.1662G>A) c.836G>A (p.Trp279Ter) c.1352G>A (p.Trp451Ter) c.1061G>A (p.Trp354Ter) c.2319+26302C>T (n.2319+26302C>T) c.896G>A (p.Trp299Ter) n.500C>T | ClinVar dbSNP |
| 9 | g.95107082C= | CA1865462118 | AOPEP,FANCC | n.410+26302C= n.2332G= c.1517G= (p.Trp506=) c.1662G= (n.1662G=) c.836G= (p.Trp279=) c.1352G= (p.Trp451=) c.1061G= (p.Trp354=) c.2319+26302C= (n.2319+26302C=) c.896G= (p.Trp299=) n.500C= | dbSNP |