exon 14
c.1927G>A
r.[1927g>a, 1755_1928del, 1889_1928del]
p.[Gly643Arg, Leu587_Ala644del, Glu630Gly*53]
Substitution
Substitution/ Splicing (exon variant)
Substitution (missense)
Pathogenic
Potentially less severe
Classic infantile
Unknown
MAF is less than 1%
rs28937909
causes partial skipping of exon 14
new cryptic splice acceptor
unknown
Disease causing (p-value: 1)
Deleterious (score: 0)
Class C65 (GV: 0.00 - GD: 125.13)
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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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