Duplication | NM_001370259.2(MEN1):c.340dup (p.Ser114fs) | MEN1 | Pathogenic | 11 | 64577241 | 64577242 | C | CT | criteria provided, multiple submitters, no conflicts | ClinGen:CA10603131 |
Duplication | NM_020975.6(RET):c.890dup (p.Val298fs) | RET | Pathogenic | 10 | 43601845 | 43601846 | C | CG | criteria provided, single submitter | ClinGen:CA10603140 |
Duplication | NM_001370259.2(MEN1):c.1429dup (p.Glu477fs) | MEN1 | Pathogenic | 11 | 64572209 | 64572210 | T | TC | criteria provided, single submitter | ClinGen:CA10603166 |
Indel | NM_001370259.2(MEN1):c.490_491delinsT (p.Ala164fs) | MEN1 | Pathogenic | 11 | 64575526 | 64575527 | GC | A | criteria provided, single submitter | ClinGen:CA10603168 |
single nucleotide variant | NM_001370259.2(MEN1):c.446-2A>C | MEN1 | Pathogenic | 11 | 64575573 | 64575573 | T | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA10603221 |
single nucleotide variant | NM_020975.6(RET):c.2418C>G (p.Tyr806Ter) | RET | Pathogenic | 10 | 43615004 | 43615004 | C | G | criteria provided, single submitter | ClinGen:CA10606962 |
Duplication | NM_001370259.2(MEN1):c.773_775dup (p.Gln258dup) | MEN1 | Likely pathogenic | 11 | 64575031 | 64575032 | A | AGCT | criteria provided, single submitter | ClinGen:CA16042754 |
Deletion | NM_001370259.2(MEN1):c.207del (p.Asp70fs) | MEN1 | Pathogenic | 11 | 64577375 | 64577375 | CG | C | criteria provided, single submitter | ClinGen:CA16042759 |
single nucleotide variant | NM_001370259.2(MEN1):c.913-1G>A | MEN1 | Pathogenic/Likely pathogenic | 11 | 64573841 | 64573841 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA16042860 |
Deletion | NM_001370259.2(MEN1):c.654+1del | MEN1 | Pathogenic | 11 | 64575362 | 64575362 | AC | A | criteria provided, single submitter | ClinGen:CA16043460 |