Total submissions: 1
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Victorian Clinical Genetics Services, |
RCV004594633 | SCV002557354 | uncertain significance | Autosomal recessive limb-girdle muscular dystrophy type 2O | 2022-09-02 | criteria provided, single submitter | clinical testing | Based on the classification scheme VCGS_Germline_v1.3.4, this variant is classified as VUS-3A. Following criteria are met: 0102 - Loss of function is a known mechanism of disease in this gene and is associated with muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3 (MIM#253280), (congenital with mental retardation), type B, 3 (MIM#613151) or (limb-girdle), type C, 3 (MIM#613157); and retinitis pigmentosa 76 (MIM#617123). (I) 0106 - This gene is associated with autosomal recessive disease. (I) 0200 - Variant is predicted to result in a missense amino acid change from serine to glycine. (I) 0251 - This variant is heterozygous. (I) 0301 - Variant is absent from gnomAD (both v2 and v3). (SP) 0309 - An alternative amino acid change at the same position has been observed in gnomAD (v2: 1 heterozygote, 0 homozygotes). (I) 0503 - Missense variant consistently predicted to be tolerated by multiple in silico tools or not conserved in placental mammals with a minor amino acid change. In addition, while this variant lies within the splice region, the nucleotide is highly conserved and abnormal splicing is not predicted. (SB) 0600 - Variant is located in the annotated GNT-I domain (DECIPHER). (I) 0703 - Another missense comparable to the one identified in this case has moderate previous evidence for pathogenicity. p.(Ser550Asn) has been reported in at least two homozygotes with peripheral hypotonia and muscle-eye-disease (PMID: 35846108 , 11709191). (SP) 0807 - This variant has no previous evidence of pathogenicity. (I) 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 |