| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.66850918C>A | CA339938 | PC | c.2229G>T (p.Met743Ile) n.290-853G>T c.*238G>T (n.*238G>T) c.*705G>T (n.*705G>T) n.842G>T c.708G>T (p.Met236Ile) c.933G>T (p.Met311Ile) c.864G>T (p.Met288Ile) | ClinVar dbSNP |
| 11 | g.66850918C= | CA1979880297 | PC | c.2229G= (p.Met743=) n.290-853G= c.*238G= (n.*238G=) c.*705G= (n.*705G=) n.842G= c.708G= (p.Met236=) c.933G= (p.Met311=) c.864G= (p.Met288=) | dbSNP |