ClinVar Miner

Submissions for variant NM_001360.2(DHCR7):c.1406G>C (p.Arg469Pro) (rs201150384)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000519844 SCV000617666 uncertain significance not provided 2017-07-03 criteria provided, single submitter clinical testing The R469P variant in the DHCR7 gene has been reported previously in a female patient with Smith-Lemli-Opitz syndrome (SLOS) who also harbored the E448K variant in unknown phase, and in a male patient with SLOS who had no second variant identified (Yu et al., 2000). The R469P variant is not observed at a significant frequency in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server). The R469P variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. In addition, this substitution occurs at a position that is conserved across species, and in silico analysis predicts this variant is probably damaging to the protein structure/function. Missense variants in nearby residues (V466M, V466A, P467L, L470Q) have been reported in the Human Gene Mutation Database in association with SLOS (Stenson et al., 2014), supporting the functional importance of this region of the protein. We interpret R469P as a variant of uncertain significance.
Counsyl RCV000670231 SCV000795061 uncertain significance Smith-Lemli-Opitz syndrome 2017-10-25 criteria provided, single submitter clinical testing

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