Description
"A Homozygote Intron, Splice site donor, c.*3_*5+1delTAAG in Exon 28 of the OPA1 gene that results in the amino acid substitution was identified. The observed variant has a minor allele frequency of 0.00003% in gnomAD exomes and genomes, respectively. The severity of the impact of this variant on the protein is high, based on the effect of the protein and REVEL score. Rare Exome Variant Ensemble Learner (REVEL) is an ensembl method for predicting the pathogenicity of missense variants based on a combination of scores from 13 individual tools: MutPred, FATHMM v2.3, VEST 3.0, PolyPhen-2, SIFT, PROVEAN, MutationAssessor, MutationTaster, LRT, GERP++, SiPhy, phyloP, and phastCons. The REVEL score for an individual missense variant can range from 0 to 1, with higher scores reflecting greater likelihood that the variant is disease-causing. ClinVar has also classified this variant as Likely Pathogenic (Variation ID: 1184587). Based on the above evidence this variant has been classified as Likely Pathogenic according to the ACMG guidelines. Mitochondrial DNA depletion syndrome-14 (MTDPS14) is caused by homozygous mutation in the OPA1 gene on chromosome 3q29. Clinical features may include hypotonia and peripheral hypertonia with opisthotonic posturing from birth, as well as feeding difficulties and profound neurodevelopmental delay, muscle wasting, sensorineural deafness, optic atrophy, and progressive cardiomyopathy."
| # | Sample | Method | Observation |
|---|
| Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences |
|---|
| 1 | germline | yes | not provided | not provided | not provided | | 1 | not provided | not provided | not provided |
