Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Department Of Translational Genomics |
RCV000171426 | SCV000221623 | likely pathogenic | not provided | criteria provided, single submitter | research | ||
| Victorian Clinical Genetics Services, |
RCV002470786 | SCV002768346 | uncertain significance | Myopathy caused by variation in FKTN | 2020-10-19 | criteria provided, single submitter | clinical testing | Based on the classification scheme VCGS_Germline_v1.3.4, this variant is classified as 3B-VUS. Following criteria are met: 0102 - Loss of function is a known mechanism of disease in this gene and is associated with Cardiomyopathy, dilated, 1X (MIM#611615), congenital muscular dystrophy type A, 4 (MIM#253800), type B, 4 (MIM#613152) and limb-girdle muscular dystophy, type C, 4 (MIM#611588) (OMIM). (I) 0106 - This gene is associated with autosomal recessive disease. (I) 0200 - Variant is predicted to result in a missense amino acid change from cysteine to phenylalanine. (I) 0251 - This variant is heterozygous. (I) 0301 - Variant is absent from gnomAD (both v2 and v3). (SP) 0501 - Missense variant consistently predicted to be damaging by multiple in silico tools and highly conserved with a major amino acid change. (SP) 0604 - Variant is not located in an established domain, motif, hotspot or informative constraint region. (I) 0705 - No comparable missense variants have previous evidence for pathogenicity. Although the p.C105Y missense variant has been classified in LOVD as likely pathogenic, there was no evidence provided to support pathogenicity and therefore could not be considered. (I) 0803 - This variant has limited previous evidence of pathogenicity in an unrelated individual. The p.Cys105Phe variant has been reported in one Limb-Girdle Muscular Dystrophy family, where muscle biopsy of the affected individual demonstrated dystrophic or myopathic changes (PMID: 27671536). (SP) 0905 - No published segregation evidence has been identified for this variant. (I) 1007 - No published functional evidence has been identified for this variant. (I) 1208 - Inheritance information for this variant is not currently available in this individual. (I) Legend: (SP) - Supporting pathogenic, (I) - Information, (SB) - Supporting benign |