Variant #0000478441 (NC_000017.10:g.78082336G>T, NM_000152.3:c.1124G>T (GAA))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.78082336G>T
DNA change (hg38) g.80108537G>T
Published as -
ISCN -
DB-ID GAA_000393 See all 4 reported entries
Variant remarks predicted potentially less severe, classic infantile phenotype when combined with null allele; predicted CRIM+ (protein expressed); Align GVGD class C65 (GV: 0.00-GD: 101.88), SIFT deleterious (score: 0), Mutation Taster disease causing (p-value: 1)
Reference Pompe disease database 731
ClinVar ID -
dbSNP ID rs142752477
Origin SUMMARY record
Segregation -
Frequency MAF <0.01
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Pim Pijnappel
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-05-09 16:06:10 +02:00 (CEST)
Date last edited 2019-06-28 11:29:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Enzyme activity     
GAA NM_000152.3 +?/. 7 c.1124G>T r.(?) p.(Arg375Leu) gives 0.3% residual activity in expression study


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