ClinVar Miner

Submissions for variant NM_173483.4(CYP4F22):c.912C>A (p.Asp304Glu)

dbSNP: rs1159994392
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004800536 SCV005421964 uncertain significance not specified 2024-10-28 criteria provided, single submitter clinical testing Variant summary: CYP4F22 c.912C>A (p.Asp304Glu) results in a conservative amino acid change in the encoded protein sequence. Four of five in-silico tools predict a damaging effect of the variant on protein function. The variant was absent in 248052 control chromosomes. The available data on variant occurrences in the general population are insufficient to allow any conclusion about variant significance. c.912C>A has been reported in the literature in an individual affected with Lamellar Ichthyosis (Hotz_2018, Hake_2022). These report(s) do not provide unequivocal conclusions about association of the variant with Lamellar Ichthyosis. To our knowledge, no experimental evidence demonstrating an impact on protein function has been reported. The following publications have been ascertained in the context of this evaluation (PMID: 34908195, 30011118). ClinVar contains an entry for this variant (Variation ID: 560323). Based on the evidence outlined above, the variant was classified as uncertain significance.
Institute for Human Genetics, University Medical Center Freiburg RCV000678416 SCV000804487 pathogenic Autosomal recessive congenital ichthyosis 5 2018-04-23 no assertion criteria provided clinical testing

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