ClinVar Miner

Submissions for variant NM_000152.5(GAA):c.872T>C (p.Leu291Pro)

dbSNP: rs2143849151
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ClinGen Lysosomal Storage Disorder Variant Curation Expert Panel RCV001789730 SCV002032137 pathogenic Glycogen storage disease, type II 2021-12-02 reviewed by expert panel curation The NM_000152.5:c.872T>C variant in GAA is a missense variant predicted to cause substitution of leucine by proline at amino acid 291 (p.Leu291Pro). At least 5 patients have been reported with this variant and features consistent with Pompe disease, including documented laboratory values showing deficiency GAA activity and/or treated with enzyme replacement therapy, and/or features consistent with infantile onset Pompe disease meeting specifications of the ClinGen LSD VCEP for PP4_Moderate (PMID 17151339, 18458862, 22353292, 22658377, 24243590, 25213570, 31193175). Additional patients have also been reported (PMID 18425781, 18458862, 29095275). Four patients are compound heterozygous for the variant and GAA variant classified as pathogenic by the ClinGen LSD VCEP, phase unknown, including c.1411_1414del (PMID 24243590; ClinVar SCV001443324.1), c.1798C>T (p.Arg600Cys)(PMID 18458862, 22353292, 25213570; 2 patients), and c.1935C>A (p.Asp645Glu)(PMID 29095275), and at least 2 patients are homozygous for the variant (PMID 16857770, 17151339, 18458862, 22658377, 31193175)(PM3_Strong). This variant is absent in gnomAD v2.1.1 (PM2_Supporting). When expressed in COS cells, this variant had 0.7% wild type GAA activity in cells and showed evidence of abnormal synthesis and processing on Western blot (PMID:22644586) (PS3_Moderate). The computational predictor REVEL gives a score of 0.908 which is above the threshold of 0.7, evidence that correlates with impact to GAA function (PP3). Two other variants have been identified at the same amino acid position, c.871C>T (p.Leu291Phe) and c.872T>A (p.Leu291His). The data from this variant, c.872T>C (p.Leu291Pro), will be used in the classification of p.Leu291Phe and p.Leu291His and is not included here to avoid circular logic. There is no entry for this variant in ClinVar. In summary, this variant meets the criteria to be classified as pathogenic for Pompe disease. GAA-specific ACMG/AMP criteria met, as specified by the ClinGen LSD VCEP (Specifications Version 2.0): PS3_Moderate, PM3_Strong, PM2_Supporting, PP3, PP4_Moderate.

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.