ClinVar Miner

Submissions for variant NM_001159699.2(FHL1):c.140_141delinsTA (p.Cys47Leu)

dbSNP: rs2148371771
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001889242 SCV002159800 uncertain significance X-linked myopathy with postural muscle atrophy 2023-12-09 criteria provided, single submitter clinical testing This sequence change replaces cysteine, which is neutral and slightly polar, with leucine, which is neutral and non-polar, at codon 31 of the FHL1 protein (p.Cys31Leu). Information on the frequency of this variant in the gnomAD database is not available, as this variant may be reported differently in the database. This variant has not been reported in the literature in individuals affected with FHL1-related conditions. ClinVar contains an entry for this variant (Variation ID: 1389420). An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be disruptive. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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