| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.87864508_87864509del | CA658657994 | PTEN | c.39_40del (p.Arg14GlufsTer29) c.39_40del (p.Arg14GlufsTer16) c.39_40del (p.Arg14GlufsTer21) c.558_559del (p.Arg187GlufsTer29) n.41_42del n.60_61del c.-64_-63del (n.-64_-63del) n.8_9del c.-667_-666del (n.-667_-666del) n.751_752del | ClinVar dbSNP |
| 10 | g.87864509dup | CA254258 | PTEN | c.40dup (p.Arg14LysfsTer30) c.40dup (p.Arg14LysfsTer17) c.40dup (p.Arg14LysfsTer22) c.559dup (p.Arg187LysfsTer30) n.42dup n.61dup c.-63dup (n.-63dup) n.9dup c.-666dup (n.-666dup) n.752dup | ClinVar dbSNP |
| 10 | g.87864508_87864509dup | CA2573145904 | PTEN | c.39_40dup (p.Arg14LysfsTer11) c.558_559dup (p.Arg187LysfsTer11) n.41_42dup n.60_61dup c.-64_-63dup (n.-64_-63dup) n.8_9dup c.-667_-666dup (n.-667_-666dup) n.751_752dup | ClinVar dbSNP |