| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.144389563del | CA273384 | ZEB2 | c.*3382del (n.*3382del) c.2756del (p.Thr919ArgfsTer?) c.3533del (p.Thr1178ArgfsTer?) c.3421del (p.Arg1141AspfsTer4) n.3502del c.3197del (p.Thr1066ArgfsTer?) c.3608del (p.Thr1203ArgfsTer?) c.*3250del (n.*3250del) n.3633del c.151+6849del (n.151+6849del) c.753del (n.753del) c.1064del (p.Thr355ArgfsTer?) c.3530del (p.Thr1177ArgfsTer?) c.656-681del (n.656-681del) c.3461del (p.Thr1154ArgfsTer?) c.3524del (p.Thr1175ArgfsTer?) c.3512del (p.Thr1171ArgfsTer?) | ClinVar dbSNP |
| 2 | g.144389563G= | CA3085660981 | ZEB2 | c.*3382C= (n.*3382C=) c.2756C= (p.Thr919=) c.3533C= (p.Thr1178=) c.3421C= (p.Arg1141=) n.3502C= c.3197C= (p.Thr1066=) c.3608C= (p.Thr1203=) c.*3250C= (n.*3250C=) n.3633C= c.151+6849C= (n.151+6849C=) c.753C= (n.753C=) c.1064C= (p.Thr355=) c.3530C= (p.Thr1177=) c.656-681C= (n.656-681C=) c.3461C= (p.Thr1154=) c.3524C= (p.Thr1175=) c.3512C= (p.Thr1171=) | dbSNP |