single nucleotide variant | NM_001267550.2(TTN):c.56648-1G>A | TTN | Likely pathogenic | 2 | 179463790 | 179463790 | C | T | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_001267550.2(TTN):c.56347+1G>A | TTN | Likely pathogenic | 2 | 179464280 | 179464280 | C | T | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_001276345.2(TNNT2):c.294T>A (p.Asp98Glu) | TNNT2 | Likely pathogenic | 1 | 201334738 | 201334738 | A | T | criteria provided, single submitter | - |
single nucleotide variant | NM_001267550.2(TTN):c.104947C>T (p.Gln34983Ter) | TTN | Likely pathogenic | 2 | 179396395 | 179396395 | G | A | criteria provided, single submitter | - |
single nucleotide variant | NM_001267550.2(TTN):c.82525C>T (p.Arg27509Ter) | TTN | Likely pathogenic | 2 | 179428334 | 179428334 | G | A | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_001267550.2(TTN):c.80950G>T (p.Glu26984Ter) | TTN | Likely pathogenic | 2 | 179429909 | 179429909 | C | A | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000256.3(MYBPC3):c.773-2A>T | MYBPC3 | Likely pathogenic | 11 | 47369458 | 47369458 | T | A | criteria provided, single submitter | - |
single nucleotide variant | NM_000256.3(MYBPC3):c.622C>T (p.Gln208Ter) | MYBPC3 | Likely pathogenic | 11 | 47371357 | 47371357 | G | A | criteria provided, single submitter | - |
Deletion | NM_020778.5(ALPK3):c.4391del (p.Asn1464fs) | ALPK3 | Pathogenic/Likely pathogenic | 15 | 85406125 | 85406125 | GA | G | criteria provided, multiple submitters, no conflicts | - |