Variant #0000168302 (NC_000017.10:g.78083828_78083831del, NM_000152.3:c.1411_1414del (GAA))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.78083828_78083831del
DNA change (hg38) g.80110029_80110032del
Published as -
ISCN -
DB-ID GAA_000053 See all 12 reported entries
Variant remarks predicted very severe, classic infantile phenotype when combined with null allele; predicted CRIM- (protein not expressed)
Reference Pompe disease database 794
ClinVar ID -
dbSNP ID rs770276275
Origin SUMMARY record
Segregation -
Frequency MAF <0.01
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Marianne Hoogeveen-Westerveld
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-04-14 13:18:39 +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 +/. 9 c.1411_1414del r.(?) p.(Glu471Profs*5) -


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