| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Duplication (frameshift variant) | not provided | Gno classifications from unflagged records |
| | | Deletion (frameshift variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (splice acceptor variant) | not provided | Gno classifications from unflagged records |
| | | Single nucleotide variant (nonsense) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant) | not provided | Gno classifications from unflagged records |
| | | Single nucleotide variant (nonsense) | Catecholaminergic polymorphic ventricular tachycardia 1 +4 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | not provided | |
| | | Deletion (frameshift variant) | not provided +3 more | |
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