single nucleotide variant | NM_001267550.2(TTN):c.94405A>T (p.Lys31469Ter) | TTN | Likely pathogenic | 2 | 179411847 | 179411847 | T | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA349474274 |
single nucleotide variant | NM_001267550.2(TTN):c.67897G>T (p.Glu22633Ter) | TTN | Likely pathogenic | 2 | 179443860 | 179443860 | C | A | criteria provided, single submitter | ClinGen:CA349422569 |
Indel | NM_001267550.2(TTN):c.73324_73328delinsC (p.Ala24442fs) | TTN | Likely pathogenic | 2 | 179437531 | 179437535 | CAGGC | G | criteria provided, single submitter | ClinGen:CA658796035 |
single nucleotide variant | NM_001267550.2(TTN):c.82350T>G (p.Tyr27450Ter) | TTN | Likely pathogenic | 2 | 179428509 | 179428509 | A | C | criteria provided, single submitter | ClinGen:CA349573976 |
single nucleotide variant | NM_001267550.2(TTN):c.60307A>T (p.Arg20103Ter) | TTN | Likely pathogenic | 2 | 179456145 | 179456145 | T | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA349485552 |
Deletion | NM_001267550.2(TTN):c.56741del (p.Ser18914fs) | TTN | Likely pathogenic | 2 | 179463696 | 179463696 | AG | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA658796055 |
single nucleotide variant | NM_001267550.2(TTN):c.58874G>A (p.Trp19625Ter) | TTN | Likely pathogenic | 2 | 179458061 | 179458061 | C | T | criteria provided, single submitter | ClinGen:CA349501161 |
Duplication | NM_001267550.2(TTN):c.48369dup (p.Glu16124fs) | TTN | Likely pathogenic | 2 | 179480458 | 179480459 | C | CT | criteria provided, single submitter | ClinGen:CA658796073 |
Duplication | NM_001267550.2(TTN):c.57035dup (p.Leu19013fs) | TTN | Likely pathogenic | 2 | 179463308 | 179463309 | T | TG | criteria provided, single submitter | ClinGen:CA658796048 |
Deletion | NM_001267550.2(TTN):c.51525del (p.Ser17177fs) | TTN | Pathogenic/Likely pathogenic | 2 | 179474625 | 179474625 | CT | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA658795993 |