Total submissions: 3
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Ai |
RCV002224608 | SCV002502191 | uncertain significance | not provided | 2022-03-07 | criteria provided, single submitter | clinical testing | |
| Fulgent Genetics, |
RCV002505886 | SCV002814554 | uncertain significance | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J; Tibial muscular dystrophy; Myopathy, myofibrillar, 9, with early respiratory failure; Early-onset myopathy with fatal cardiomyopathy; Hypertrophic cardiomyopathy 9 | 2021-08-30 | criteria provided, single submitter | clinical testing | |
| Broad Center for Mendelian Genomics, |
RCV003225988 | SCV003922166 | uncertain significance | Autosomal recessive limb-girdle muscular dystrophy type 2J | 2023-05-02 | criteria provided, single submitter | curation | The heterozygous p.Pro12394AlafsTer18 variant in TTN was identified by our study, in the compound heterozygous state with a likely pathogenic variant (ClinVar Variation ID: 288119), in two siblings with limb-girdle muscular dystrophy. Familial exome analysis revealed that this variant was in trans with a likely pathogenic variant (ClinVar Variation ID: 288119). The p.Pro12394AlafsTer18 variant in TTN has been previously reported in individuals with autosomal recessive limb girdle muscular dystrophy 10 but has been identified in 0.002% (1/48292) of European (Finnish) chromosomes by the Genome Aggregation Database (gnomAD, http://gnomad.broadinstitute.org; dbSNP ID: rs2064831878). Although this variant has been seen in the general population in a heterozygous state, its frequency is low enough to be consistent with a recessive carrier frequency. This variant has also been reported in ClinVar (Variation ID: 1678017) and has been interpreted as a variant of uncertain significance by AiLife Diagnostics and Fulgent Genetics. This variant is predicted to cause a frameshift, which alters the protein’s amino acid sequence beginning at position 12394 and leads to a premature termination codon 18 amino acids downstream. This alteration is then predicted to lead to a truncated or absent protein. Loss of function of the TTN gene is an established disease mechanism in autosomal recessive limb girdle muscular dystrophy 10. Conservation and expression data indicate that this exon might not be biologically relevant for this disease, and therefore this variant is not expected to result in loss of function of TTN. In summary, the clinical significance of the p.Pro12394AlafsTer18 variant is uncertain. ACMG/AMP Criteria applied: PM2_Supporting, PM3 (Richards 2015). |