Deletion | NM_001267550.2(TTN):c.52576_52603del (p.Asn17525_Ala17526insTer) | TTN | Likely pathogenic | 2 | 179473007 | 179473034 | AATAAGCCATCTACATTGGCTTTCAAGGC | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA16610476 |
single nucleotide variant | NM_001267550.2(TTN):c.15496+1G>T | TTN | Pathogenic/Likely pathogenic | 2 | 179599054 | 179599054 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA16610517 |
Deletion | NC_000011.10:g.(?_47349774)_(47351505_?)del | MYBPC3 | Pathogenic | 11 | 47371325 | 47373056 | na | na | criteria provided, single submitter | - |
Deletion | NC_000011.10:g.(?_47331845)_(47336011_?)del | MYBPC3 | Pathogenic | 11 | 47353396 | 47357562 | na | na | criteria provided, single submitter | - |
Deletion | NM_000256.3(MYBPC3):c.3665del (p.Gly1222fs) | MYBPC3 | Pathogenic | 11 | 47353772 | 47353772 | TC | T | criteria provided, single submitter | ClinGen:CA16613340 |
Deletion | NM_000256.3(MYBPC3):c.3617del (p.Gly1206fs) | MYBPC3 | Pathogenic | 11 | 47354127 | 47354127 | AC | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA16613343 |
Insertion | NM_000256.3(MYBPC3):c.2572_2573insAA (p.Ser858fs) | MYBPC3 | Pathogenic | 11 | 47358971 | 47358972 | C | CTT | criteria provided, single submitter | ClinGen:CA16613382 |
Deletion | NM_000256.3(MYBPC3):c.2279del (p.Asp760fs) | MYBPC3 | Pathogenic | 11 | 47360100 | 47360100 | GT | G | criteria provided, single submitter | ClinGen:CA16613383 |
Indel | NM_000256.3(MYBPC3):c.257_259delinsGGAGG (p.Ser86fs) | MYBPC3 | Pathogenic | 11 | 47372823 | 47372825 | TGG | CCTCC | criteria provided, single submitter | ClinGen:CA16613417 |
Deletion | NC_000012.12:g.(?_110910819)_(110911175_?)del | MYL2 | Pathogenic | 12 | 111348623 | 111348979 | na | na | criteria provided, single submitter | - |