Variant #0000168292 (NC_000017.10:g.78086826G>A, NM_000152.3:c.2040G>A (GAA))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.78086826G>A
DNA change (hg38) g.80113027G>A
Published as -
ISCN -
DB-ID GAA_000231 See all 3 reported entries
Variant remarks predicted less severe phenotype, childhood phenotype when combined with null allele; predicted CRIM? (protein expression unknown)
Reference Pompe disease database 956
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency MAF not reported
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 2025-06-09 06:38:10 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Enzyme activity     
GAA NM_000152.3 ?/. 14 c.2040G>A r.(?) p.(=) -


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