Total submissions: 1
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Victorian Clinical Genetics Services, |
RCV002471956 | SCV002767633 | pathogenic | Stickler syndrome, type I, nonsyndromic ocular | 2021-05-06 | criteria provided, single submitter | clinical testing | Based on the classification scheme VCGS_Germline_v1.1.1, this variant is classified as Pathogenic. Following criteria are met: 0102 - Loss-of-function is a known mechanism of disease for this gene. (N) Variants resulting in a premature termination codon have been shown to result in haploinsufficiency (PMID: 17721977, PMID: 27234559, PMID: 20179744). (N) 0104 - Dominant Negative is a mechanism of disease for this gene. (N) Missense variants affecting glycine residues have been shown to cause a dominant negative disease mechanism (PMID: 15895462). (N) 0107 - This gene is known to be associated with autosomal dominant disease. However some cases of autosomal recessive inheritance have also been reported (PMID: 25060605, 26358419). (N) 0201 - Variant is predicted to cause nonsense-mediated decay (NMD) and loss of protein (exon 8 of 54). (P) 0251 - Variant is heterozygous. (N) 0301 - Variant is absent from gnomAD. (P) 0701 - Comparable variants have very strong previous evidence for pathogenicity. Other variants predicted to cause NMD have been reported as pathogenic (ClinVar). (P) 0807 - Variant has not previously been reported in a clinical context. (N) 0905 - No segregation evidence has been identified for this variant. (N) 1007 - No published functional evidence has been identified for this variant. (N) 1206 - Variant is paternally inherited. (N) Legend: (P) - Pathogenic, (N) - Neutral, (B) - Benign |