Deletion | NM_000256.3(MYBPC3):c.3662del (p.Leu1221fs) | MYBPC3 | Pathogenic/Likely pathogenic | 11 | 47353775 | 47353775 | CA | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA279321 |
Duplication | NM_000256.3(MYBPC3):c.3414dup (p.Val1139fs) | MYBPC3 | Likely pathogenic | 11 | 47354440 | 47354441 | C | CG | criteria provided, multiple submitters, no conflicts | ClinGen:CA279290 |
single nucleotide variant | NM_000256.3(MYBPC3):c.3300C>A (p.Tyr1100Ter) | MYBPC3 | Pathogenic/Likely pathogenic | 11 | 47354775 | 47354775 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA279299 |
Duplication | NM_000256.3(MYBPC3):c.2670dup (p.Arg891fs) | MYBPC3 | Likely pathogenic | 11 | 47357494 | 47357495 | G | GC | criteria provided, single submitter | ClinGen:CA279270 |
Deletion | NM_000256.3(MYBPC3):c.2550del (p.Asn850fs) | MYBPC3 | Likely pathogenic | 11 | 47358994 | 47358994 | CG | C | criteria provided, single submitter | ClinGen:CA279283 |
single nucleotide variant | NM_000256.3(MYBPC3):c.2376G>A (p.Trp792Ter) | MYBPC3 | Pathogenic/Likely pathogenic | 11 | 47359278 | 47359278 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA279280 |
single nucleotide variant | NM_000256.3(MYBPC3):c.2371C>T (p.Gln791Ter) | MYBPC3 | Pathogenic/Likely pathogenic | 11 | 47359283 | 47359283 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA279318 |
Deletion | NM_000256.3(MYBPC3):c.306del (p.Met103fs) | MYBPC3 | Likely pathogenic | 11 | 47372153 | 47372153 | TG | T | criteria provided, single submitter | ClinGen:CA279289 |
Duplication | NM_000256.3(MYBPC3):c.227dup (p.Ser78fs) | MYBPC3 | Likely pathogenic | 11 | 47372854 | 47372855 | C | CT | criteria provided, single submitter | ClinGen:CA279311 |
single nucleotide variant | NM_000257.4(MYH7):c.3358G>A (p.Glu1120Lys) | MYH7 | Likely pathogenic | 14 | 23889422 | 23889422 | C | T | criteria provided, single submitter | ClinGen:CA279329 |