single nucleotide variant | NM_170707.4(LMNA):c.784G>T (p.Glu262Ter) | LMNA | Likely pathogenic | 1 | 156104740 | 156104740 | G | T | criteria provided, single submitter | ClinGen:CA018633 |
Deletion | NM_170707.4(LMNA):c.763del (p.Gln255fs) | LMNA | Likely pathogenic | 1 | 156104718 | 156104718 | AC | A | criteria provided, single submitter | ClinGen:CA018586 |
single nucleotide variant | NM_170707.4(LMNA):c.745C>G (p.Arg249Gly) | LMNA | Likely pathogenic | 1 | 156104701 | 156104701 | C | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA018552 |
single nucleotide variant | NM_170707.4(LMNA):c.513+1G>C | LMNA | Likely pathogenic | 1 | 156100565 | 156100565 | G | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA018184 |
single nucleotide variant | NM_170707.4(LMNA):c.154C>G (p.Leu52Val) | LMNA | Likely pathogenic | 1 | 156084863 | 156084863 | C | G | criteria provided, single submitter | ClinGen:CA017415 |
single nucleotide variant | NM_021629.4(GNB4):c.158G>A (p.Gly53Asp) | GNB4 | Likely pathogenic | 3 | 179137232 | 179137232 | C | T | criteria provided, single submitter | ClinGen:CA130933,UniProtKB:Q9HAV0#VAR_069908,OMIM:610863.0001 |
single nucleotide variant | NM_025137.4(SPG11):c.1679C>G (p.Ser560Ter) | SPG11 | Likely pathogenic | 15 | 44925759 | 44925759 | G | C | criteria provided, single submitter | ClinGen:CA344304 |
single nucleotide variant | NM_000530.8(MPZ):c.89T>C (p.Ile30Thr) | MPZ | Likely pathogenic | 1 | 161277193 | 161277193 | A | G | criteria provided, single submitter | ClinGen:CA343888 |
single nucleotide variant | NM_018706.7(DHTKD1):c.1455T>G (p.Tyr485Ter) | DHTKD1 | Likely pathogenic | 10 | 12139779 | 12139779 | T | G | criteria provided, single submitter | ClinGen:CA130364,OMIM:614984.0004 |
single nucleotide variant | NM_002437.5(MPV17):c.509C>T (p.Ser170Phe) | MPV17 | Likely pathogenic | 2 | 27532802 | 27532802 | G | A | criteria provided, single submitter | ClinGen:CA342985 |