Link to Pubmed | Location | DNA nomenclature | RNA nomenclature | Protein nomenclature | Type of variant DNA | Type of variant RNA | Type of variant Protein | MAF | RS number | Biochemical evidence of pathogenicity | Splicing and translation prediction | Biochemical evidence of CRIM status | Prediction of CRIM status | Number of patients | Id | Predicted severity | Phenotype with null allele | CRIM status | Missense prediction (Mutation Taster) | Missense prediction (SIFT) | Missense prediction (Align GVGD) |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
PubMed | exon 8 | c.1309C>T | r.(1309c>u) | p.(Arg437Cys) | Substitution | Substitution | Substitution (missense) | MAF is less than 1% | rs770610356 | no effect on splicing | protein is expressed | 365 | Less severe | Childhood | Positive | Disease causing (p-value: 0.998) | Deleterious (score: 0.01) | Class C15 (GV: 98.89 - GD: 126.72) | |||
Link to patients |
Allele 1 DNA |
Allele 2 Location |
Allele 2 DNA |
Allele 2 Phenotype with a null allele |
Phenotype of patient |
Age of Onset |
Gender |
Age at analysis |
Cardiomyopathy |
Liver/ Spleen |
Ventilatory support |
Respiratory problems |
Wheelchair dependency |
Mobility problems |
(Kypho) Scoliosis |
Ptosis |
Scapular winging |
Cerebral vessels anomalies |
No of patients reported |
Country/Region | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
PubMed | c.1309C>T | exon 4 | c.796C>T | Classic infantile | Childhood | 8 years | M | 14 years | - | 1 | China | ||||||||||
PubMed | c.1309C>T | exon 7 | c.1082C>T | Classic infantile | Childhood (1)/ unknown (1) | early childhood/asymptomatic | M/ M | 16 years/13 years | -/- | + at night/- | +/- | +/- | +/- | 2 | China | ||||||
PubMed | c.1309C>T | exon 16 | c.2326C>T | Unknown (disease-associated) | Childhood | <7 years/<7 years | F/ F | 11 years/10 years | + at night/+ at night | +/+ | -/- | +/+ | +/+ | 2 | Japan | ||||||
PubMed | c.1309C>T | exon 8 | c.1309C>T | Childhood | Adult | 20 years | M | 30 years | - | + | + | + | 1 | Japan | |||||||
PubMed | c.1309C>T | exon 10 | c.1544T>A | Unknown (disease-associated) | Adult | 18 years | M | 23 years | incomplete right bundle branch block | + at night | + | - | - | 1 | Japan | ||||||
PubMed | c.1309C>T | exon 13 | c.1822C>T | Classic infantile | Childhood | 15 months | M | 2,7 years | - | + | 1 | Korea | |||||||||
PubMed | c.1309C>T | exon 4 | c.796C>T | Classic infantile | Childhood | 8 years | M | unknown | + | 1 | China | ||||||||||
PubMed | c.1309C>T | exon 15 | c.2177C>G | Childhood | Childhood | 1-2 years and 4 months | F | 2 years,4 months | - | + | - | - | 1 | Japan | |||||||
PubMed | c.1309C>T | exon 13 | c.1798C>T | Classic infantile | Childhood (3) | <1 years/ 3 years/ 8 years | F/NA/M | -/NA/- | -/NA/- | -/NA/- | -/NA/+ | -/NA/+ | 3 | Japan | |||||||
PubMed | c.1309C>T | exon 16 | c.2297A>G | Childhood or adult | Childhood | 14 years | M | 21 years | - | - | + | + | - | 1 | Japan | ||||||
PubMed | c.1309C>T | exon 13 | c.1857C>G | Classic infantile or Childhood | Adult | 19 years | F | + | + | + | + | + | 1 | Japan | |||||||
PubMed | c.1309C>T | exon 15 | c.2051C>A | Unknown (disease-associated) | Adult | 19 years | F | 22 years/29 years | 1 | China | |||||||||||
PubMed | c.1309C>T | exon 7 | c.1082C>T | Classic infantile | Childhood | 6 years/10 years | M/M | 9 years/15 years | -/+ | -/+ | 2 | Hong Kong | |||||||||
PubMed | c.1309C>T | exon 16 | c.2238G>C | Childhood or Adult | Childhood | 16 years | M | 26 years | - | - | 1 | Hong Kong | |||||||||
PubMed | c.1309C>T | exon 15 | c.2177C>G | Childhood | Childhood | 1 years | F | - | + | - | - | - | 1 | Japan | |||||||
PubMed | c.1309C>T | exon 13 | c.1822C>T | Classic infantile | Childhood | 1 years | M | 2 y, 9 m | - | + (hepatomegaly) | + (tracheostomy at 5 y, 7 m) | + | + (at 6y, 2m) | Limb girdle weakness | + | 1 | Korea | ||||
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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