Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.1220448dup | CA645369765 | STK11 | c.540dup (p.Asn181GlufsTer?) c.168dup (p.Asn57GlufsTer?) c.366dup (p.Asn123GlufsTer?) n.363dup n.630dup n.436dup c.318dup (p.Asn107GlufsTer?) n.1165dup | ClinVar dbSNP |
19 | g.1220448del | CA658824798 | STK11 | c.540del (p.Asn181ThrfsTer?) c.168del (p.Asn57ThrfsTer?) c.366del (p.Asn123ThrfsTer?) n.363del n.630del n.436del c.318del (p.Asn107ThrfsTer?) n.1165del | ClinVar dbSNP |