Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Women's Health and Genetics/Laboratory Corporation of America, |
RCV005240452 | SCV005886402 | pathogenic | Lamellar ichthyosis | 2025-02-17 | criteria provided, single submitter | clinical testing | Variant summary: CYP4F22 c.242G>A (p.Gly81Asp) results in a non-conservative amino acid change in the encoded protein sequence. Three of five in-silico tools predict a damaging effect of the variant on protein function. The variant was absent in 251438 control chromosomes. c.242G>A has been reported in the literature in individuals affected with Lamellar Ichthyosis (e.g. Hotz_2018, Diociaiuti_2024). These data indicate that the variant is likely to be associated with disease. At least one publication reports experimental evidence evaluating an impact on protein function and found that the variant results in <10% of WT enzyme activity (Nohara_2021). The following publications have been ascertained in the context of this evaluation (PMID: 30011118, 38588653, 33067036). ClinVar contains an entry for this variant (Variation ID: 560306). Based on the evidence outlined above, the variant was classified as pathogenic. |
| Institute for Human Genetics, |
RCV000678397 | SCV000804468 | pathogenic | Autosomal recessive congenital ichthyosis 5 | 2018-04-23 | no assertion criteria provided | clinical testing |