Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000669490 | SCV000794247 | uncertain significance | Holocarboxylase synthetase deficiency | 2017-09-20 | criteria provided, single submitter | clinical testing | |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV000669490 | SCV002570590 | likely pathogenic | Holocarboxylase synthetase deficiency | 2022-07-18 | criteria provided, single submitter | clinical testing | Variant summary: HLCS c.1409T>C (p.Leu470Ser) results in a non-conservative amino acid change located in the biotinyl protein ligase (BPL) and lipoyl protein ligase (LPL), catalytic domain (IPR004143) of the encoded protein sequence. Five of five in-silico tools predict a damaging effect of the variant on protein function. The variant was absent in 251462 control chromosomes (gnomAD). c.1409T>C has been reported in the literature in at least one compound heterozygous individual affected with Holocarboxylase Synthetase Deficiency (e.g. Yang_2001). In an experimental study the variant protein was found to have approximately 4% enzyme activity compared to the wild-type, suggesting the variant impairs protein function (Yang_2001). One clinical diagnostic laboratory has submitted an assessment for this variant to ClinVar after 2014 and classified the variant as uncertain significance. Based on the evidence outlined above, the variant was classified as likely pathogenic. |