| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.64807651del | CA16619362 | MEN1 | c.699del (p.Met233IlefsTer?) c.670del (p.Ala224ArgfsTer?) c.684del (p.Met228IlefsTer?) c.431del c.35del n.716del n.646del n.344del n.724del n.961del c.410del c.579del (p.Met193IlefsTer?) | ClinVar dbSNP |
| 11 | g.64807651C= | CA1978892137 | MEN1 | c.699G= (p.Met233=) c.670G= (p.Ala224=) c.684G= (p.Met228=) c.431G= c.35G= n.716G= n.646G= n.344G= n.724G= n.961G= c.410G= c.579G= (p.Met193=) | dbSNP dbSNP |