ClinVar Miner

Submissions for variant NM_000152.5(GAA):c.2167_2179delinsTGCGACGTGG (p.Val723_Leu727delinsCysAspValVal)

dbSNP: rs2039292050
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ClinGen Lysosomal Storage Disorder Variant Curation Expert Panel RCV001200865 SCV001371735 pathogenic Glycogen storage disease, type II 2020-04-06 reviewed by expert panel curation This variant, c.2167_2179delinsTGCGACGTGG, is predicted to result in the in frame deletion of five amino acids (ValAlaArgProLeu) and insertion of another four amino acids in GAA (p.Val723_LeudelinsCysAspValVal), meeting PM4. The variant is absent in gnomAD v2.1.1, meeting PM2. To our knowledge, this variant has not been reported in the literature in individuals with Pompe disease, and experimental studies are not available. However, there is unpublished clinical laboratory data on two patients with the variant who have deficient GAA activity in dried blood spots, meeting PP4. One is compound heterozygous for the variant and c.-32-13T>G (known pathogenic variant), the other is compound heterozygous for the variant and c.655G>A (p.Gly219Arg) (pathogenic based on assessment by the ClinGen LSD VCEP). In both cases, the variants are confirmed in trans. This data meets PM3_Strong. PROVEAN and Mutation Taster predict that this variant impacts the function of GAA, meeting PP3. There is no entry for this variant in ClinVar. In summary, this variant meets the criteria to be classified as likely pathogenic for Pompe disease. GAA-specific ACMG/AMP criteria applied, as specified by the ClinGen LSD VCEP: PM2, PM4, PP3, PP4.
Revvity Omics, Revvity RCV003142126 SCV003822596 pathogenic not provided 2022-07-05 criteria provided, single submitter clinical testing

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