| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.60222677C>T | CA128507 | CA8 | c.710G>A (p.Arg237Gln) n.948G>A n.482G>A c.614G>A (p.Arg205Gln) n.986G>A c.458G>A (p.Arg153Gln) n.963G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 8 | g.60222677C= | CA1787849328 | CA8 | c.710G= (p.Arg237=) n.948G= n.482G= c.614G= (p.Arg205=) n.986G= c.458G= (p.Arg153=) n.963G= | dbSNP |