Variant #0000168232 (NC_000017.10:g.78079669G>A, NM_000152.3:c.668G>A (GAA))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.78079669G>A
DNA change (hg38) g.80105870G>A
Published as 668A>G (His223Arg)
ISCN -
DB-ID GAA_000038 See all 9 reported entries
Variant remarks predicted non-pathogenic, unknown phenotype when combined with null allele; predicted CRIM+ (protein expressed); Align GVGD class C0 (GV: 102.71-GD: 0.00), SIFT tolerated (score: 0.07), Mutation Taster polymorphism (p-value: 1)
Reference Pompe disease database 639
ClinVar ID -
dbSNP ID rs1042395
Origin SUMMARY record
Segregation -
Frequency MAF >0.05
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.66752 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 2025-06-09 03:01:54 +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 -/. 3 c.668G>A r.(?) p.(Arg223His) -


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