ClinVar Miner

Submissions for variant NC_000011.10:g.(?_22272764)_(22276219_?)del

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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 RCV000708119 SCV000837229 likely pathogenic Gnathodiaphyseal dysplasia; Autosomal recessive limb-girdle muscular dystrophy type 2L 2018-01-24 criteria provided, single submitter clinical testing This variant is an out-of-frame deletion of the genomic region encompassing exons 19-21 of the ANO5 gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 237 amino acids of the ANO5 protein. This variant has not been reported in the literature in individuals with ANO5-related disease. A different variant in the disrupted region (p.His841Asp) has been determined to be likely pathogenic (PMID: 23606453, 24022920). This suggests that this region is critical for ANO5 protein function and that other variants that disrupt it may also be pathogenic. In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic.

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