ClinVar Miner

Submissions for variant NM_004393.6(DAG1):c.1793G>A (p.Arg598His)

gnomAD frequency: 0.00001  dbSNP: rs201268364
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001863333 SCV002114500 uncertain significance Autosomal recessive limb-girdle muscular dystrophy type 2P; Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9 2021-10-06 criteria provided, single submitter clinical testing This sequence change replaces arginine with histidine at codon 598 of the DAG1 protein (p.Arg598His). The arginine residue is moderately conserved and there is a small physicochemical difference between arginine and histidine. This variant is present in population databases (rs201268364, ExAC 0.002%). This variant has not been reported in the literature in individuals affected with DAG1-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. 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.
Revvity Omics, Revvity RCV003146261 SCV003830406 uncertain significance not provided 2019-10-16 criteria provided, single submitter clinical testing

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