Total submissions: 1
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Victorian Clinical Genetics Services, |
RCV004788372 | SCV005400188 | likely pathogenic | Mitochondrial disease | 2023-07-17 | criteria provided, single submitter | clinical testing | Based on the classification scheme VCGS_Germline_v1.3.4, this variant is classified as Likely pathogenic. Following criteria are met: 0102 - Loss of function is a known mechanism of disease in this gene and is associated with mitochondrial disease MONDO:0044970, MRPL39-related. (I) 0106 - This gene is associated with autosomal recessive disease. (I) 0205 - Variant is predicted to result in a truncated protein with less than 1/3 of the protein sequence affected. RNASeq performed in a research setting indicates that this allele escapes nonsense-mediated decay (NMD). The likely, but unconfirmed, mechanism of NMD-escape for this allele is re-initiation of translation at a downstream start codon (Met43). The resulting protein would lack the N-terminal 42 residues. (SP) 0251 - This variant is heterozygous. (I) 0304 - Variant is present in gnomAD <0.01 for a recessive condition (1 heterozygote, 0 homozygotes). (SP) 0705 - No comparable NMD-escape variants have previous evidence for pathogenicity. One NMD-escape variant resulting in a C-terminal truncation has been reported; the other loss of function variants reported were confirmed to result in NMD (PMID: 37133451). (I) 0807 - This variant has no previous evidence of pathogenicity. (I) 0905 - No published segregation evidence has been identified for this variant. (I) 1010 - Functional evidence for this variant is inconclusive, but supportive of MRPL39-related mitochondrial disease. Proteomic data for this patient is indicative of mitoribosome destablisation which is consistent with what has been reported previously for patients with MRPL39-related mitochondrial disease (Stroud lab, personal communication). However, these data are not specific to MRPL39. (I) 1201 - Heterozygous variant detected in trans with a second pathogenic heterozygous variant (c.589-924G>A) in a recessive disease. (SP) 1205 - This variant has been shown to be maternally inherited by (trio analysis). (I) Legend: (SP) - Supporting pathogenic, (I) - Information, (SB) - Supporting benign |