Duplication | NM_003319.4(TTN):c.63583dup (p.Tyr21195fs) | TTN | Likely pathogenic | 2 | 179416848 | 179416849 | T | TA | criteria provided, single submitter | ClinGen:CA261916 |
single nucleotide variant | NM_001267550.2(TTN):c.81532G>T (p.Glu27178Ter) | TTN | Likely pathogenic | 2 | 179429327 | 179429327 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA261909 |
Duplication | NM_001267550.2(TTN):c.69458_69461dup (p.Asn23154fs) | TTN | Likely pathogenic | 2 | 179441509 | 179441510 | G | GTTCT | criteria provided, multiple submitters, no conflicts | ClinGen:CA261900 |
Deletion | NM_001267550.2(TTN):c.57995del (p.His19332fs) | TTN | Likely pathogenic | 2 | 179459226 | 179459226 | GT | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA261889 |
Deletion | NM_001267550.2(TTN):c.57215del (p.Gly19072fs) | TTN | Likely pathogenic | 2 | 179462682 | 179462682 | TC | T | criteria provided, single submitter | ClinGen:CA261882 |
Duplication | NM_001256850.1(TTN):c.51809dup (p.Asp17270fs) | TTN | Likely pathogenic | 2 | 179463704 | 179463705 | A | AT | criteria provided, multiple submitters, no conflicts | ClinGen:CA261881 |
single nucleotide variant | NM_001267550.2(TTN):c.56647+1G>A | TTN | Likely pathogenic | 2 | 179463872 | 179463872 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA261880 |
single nucleotide variant | NM_001267550.2(TTN):c.50618G>A (p.Trp16873Ter) | TTN | Likely pathogenic | 2 | 179476338 | 179476338 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA261872 |
single nucleotide variant | NM_001267550.2(TTN):c.47506C>T (p.Gln15836Ter) | TTN | Likely pathogenic | 2 | 179482572 | 179482572 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA261868 |
single nucleotide variant | NM_001267550.2(TTN):c.46782C>A (p.Tyr15594Ter) | TTN | Likely pathogenic | 2 | 179483495 | 179483495 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA261864 |