intron 10
c.1552-3C>G
r.[=,1551ins30, 1551ins100]
p.[(=), (Val480_Ile517del), (Ile517_Asp518insSerHisLeuProAlaAlaLeuLeuLeuGln)]
Substitution
Substitution/ Splicing (intron variant)
Deletion/ Insertion
Likely pathogenic
Potentially mild
Unknown (disease-associated)
Positive
MAF is less than 1%
rs375470378
full and partial exon 10 skip and intron 10 inclusion
weakens exon 11 splice acceptor
detection of leaky wildtype splicing
unknown
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The Pompe disease GAA variant database represents an effort to collect all known variants in the GAA gene and is maintained and provide by the Pompe center, Erasmus MC. We kindly ask you to reference one of the following articles if you use this database for research purposes: de Faria, DOS, in 't Groen, SLM, Bergsma, AJ, et al. Update of the Pompe variant database for the prediction of clinical phenotypes: Novel disease-associated variants, common sequence variants, and results from newborn screening. Niño, MY, in 't Groen, SLM, Hoogeveen-Westerveld, M, et al. Extension of the Pompe mutation database by linking disease‐associated variants to clinical severity. Human Mutation. 2019; 40: 1954–1967. https://doi.org/10.1002/humu.23854 |
www.pompecenter.nl |
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