Duplication | NM_001267550.2(TTN):c.71202dup (p.Lys23735fs) | TTN | Pathogenic/Likely pathogenic | 2 | 179439656 | 179439657 | T | TG | criteria provided, multiple submitters, no conflicts | ClinGen:CA430257756 |
Deletion | NM_001267550.2(TTN):c.60902del (p.Ser20301fs) | TTN | Likely pathogenic | 2 | 179455550 | 179455550 | AC | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA658657141 |
Deletion | NM_001267550.2(TTN):c.57849del (p.Val19284fs) | TTN | Likely pathogenic | 2 | 179459372 | 179459372 | CA | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA1992974 |
single nucleotide variant | NM_000256.3(MYBPC3):c.2738-1G>A | MYBPC3 | Likely pathogenic | 11 | 47356761 | 47356761 | C | T | criteria provided, single submitter | ClinGen:CA380316885 |
single nucleotide variant | NM_000256.3(MYBPC3):c.2526C>A (p.Tyr842Ter) | MYBPC3 | Pathogenic | 11 | 47359018 | 47359018 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA380318189 |
single nucleotide variant | NM_000256.3(MYBPC3):c.2067+1G>A | MYBPC3 | Pathogenic | 11 | 47361201 | 47361201 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA380321286 |
single nucleotide variant | NM_000257.4(MYH7):c.1052A>C (p.Lys351Thr) | MYH7 | Likely pathogenic | 14 | 23899070 | 23899070 | T | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA389051463 |
single nucleotide variant | NM_020778.5(ALPK3):c.2407C>T (p.Gln803Ter) | ALPK3 | Likely pathogenic | 15 | 85400376 | 85400376 | C | T | criteria provided, single submitter | ClinGen:CA393357038 |
single nucleotide variant | NM_001276345.2(TNNT2):c.565T>G (p.Ser189Ala) | TNNT2 | Likely pathogenic | 1 | 201332459 | 201332459 | A | C | criteria provided, single submitter | ClinGen:CA35420183 |
Deletion | NM_001267550.2(TTN):c.99588_99595del (p.Phe33196fs) | TTN | Likely pathogenic | 2 | 179402339 | 179402346 | CCAGGATGG | C | criteria provided, single submitter | ClinGen:CA658657126 |