single nucleotide variant | NM_001267550.2(TTN):c.2089A>T (p.Lys697Ter) | TTN | Likely pathogenic | 2 | 179650856 | 179650856 | T | A | criteria provided, single submitter | ClinGen:CA349502198 |
Deletion | NM_000256.3(MYBPC3):c.3627+2del | MYBPC3 | Pathogenic | 11 | 47354115 | 47354115 | TA | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA658797619 |
single nucleotide variant | NM_000256.3(MYBPC3):c.3491-2A>C | MYBPC3 | Likely pathogenic | 11 | 47354255 | 47354255 | T | G | criteria provided, single submitter | ClinGen:CA380312951 |
single nucleotide variant | NM_000256.3(MYBPC3):c.3331-1G>C | MYBPC3 | Pathogenic/Likely pathogenic | 11 | 47354525 | 47354525 | C | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA380313881 |
single nucleotide variant | NM_000256.3(MYBPC3):c.3330+1G>T | MYBPC3 | Pathogenic/Likely pathogenic | 11 | 47354744 | 47354744 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA380314001 |
single nucleotide variant | NM_000256.3(MYBPC3):c.3294G>A (p.Trp1098Ter) | MYBPC3 | Pathogenic | 11 | 47354781 | 47354781 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA053346 |
Insertion | NM_000256.3(MYBPC3):c.3228_3229insT (p.Ala1077fs) | MYBPC3 | Pathogenic | 11 | 47354846 | 47354847 | C | CA | criteria provided, single submitter | ClinGen:CA658797620 |
Insertion | NM_000256.3(MYBPC3):c.2604_2605insA (p.Pro869fs) | MYBPC3 | Pathogenic | 11 | 47357560 | 47357561 | G | GT | criteria provided, single submitter | ClinGen:CA658797622 |
Deletion | NM_000256.3(MYBPC3):c.2451del (p.Trp818fs) | MYBPC3 | Pathogenic | 11 | 47359093 | 47359093 | AC | A | criteria provided, single submitter | ClinGen:CA658797624 |
Deletion | NM_000256.3(MYBPC3):c.2310del (p.Asp770fs) | MYBPC3 | Pathogenic | 11 | 47359344 | 47359344 | CG | C | criteria provided, single submitter | ClinGen:CA658797627 |