Description
Variant summary: GBA c.970C>T (p.Arg324Cys) results in a non-conservative amino acid change located in the Glycosyl hydrolase family 30, TIM-barrel domain (IPR033453) of the encoded protein sequence. Five of five in-silico tools predict a damaging effect of the variant on protein function. The variant allele was found at a frequency of 2e-05 in 251034 control chromosomes. c.970C>T has been reported in the literature as a compound heterozygous genotype in multiple individuals predominantly affected with Type I Gaucher Disease (example, Beutler_1994, Cormand_1998, Filocamo_2002, Miocic_2005, Baris_2016, Verma_2021). These data indicate that the variant is very likely to be associated with disease. To our knowledge, no variant specific experimental evidence demonstrating an impact on protein function has been reported. Although compound heterozygous individuals with this variant demonsrated decreased residual beta glucosidase enzyme activity, elevated Lyso GL-1 biomarker levels and elevated Chitotriosidase biomarker levels (example, Verma_2021). No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar after 2014. Based on the evidence outlined above, the variant was classified as pathogenic.
# | Sample | Method | Observation |
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Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences |
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1 | germline | unknown | not provided | not provided | not provided | | not provided | not provided | not provided | not provided |