| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | TTN, TTN-AS1 (K27023fs +5 more) | Deletion (frameshift variant) | Autosomal recessive titinopathy +8 more | |
| | TTN, TTN-AS1 (K35513E +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | |
| | TTN, TTN-AS1 (E23411fs +5 more) | Duplication (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +7 more | GPathogenic/Likely pathogenic |
| | TTN-AS1, TTN (R27933C +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1G +5 more | |
| | | Single nucleotide variant (intron variant) | not provided +9 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant +1 more) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | GConflicting classifications of pathogenicity |
| | LOC101927055, TTN (I1567T +1 more) | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1G +7 more | |
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