Variant #0000168297 (NC_000017.10:g.78092118C>T, NM_000152.3:c.2608C>T (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.78092118C>T
DNA change (hg38) g.80118319C>T
Published as -
ISCN -
DB-ID GAA_000234 See all 11 reported entries
Variant remarks predicted very severe, classic infantile phenotype when combined with null allele; predicted CRIM- (no endogenous protein on Western blot)
Reference Pompe disease database 1049
ClinVar ID -
dbSNP ID rs780321415
Origin SUMMARY record
Segregation -
Frequency MAF <0.01
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-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 2025-03-13 12:24:17 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Enzyme activity     
GAA NM_000152.3 +/. 18 c.2608C>T r.(?) p.(Arg870*) no protein on western blot


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.