Variant #0000478381 (NC_000017.10:g.78079597A>G, NM_000152.3:c.596A>G (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.78079597A>G
DNA change (hg38) g.80105798A>G
Published as -
ISCN -
DB-ID GAA_000004 See all 8 reported entries
Variant remarks predicted non-pathogenic, unknown phenotype when combined with null allele; predicted CRIM+ (protein expressed); Align GVGD class C0 (GV: 113.73-GD: 0.00), SIFT tolerated (score: 0.84), Mutation Taster polymorphism (p-value: 1)
Reference Pompe disease database 633
ClinVar ID -
dbSNP ID rs528367092
Origin SUMMARY record
Segregation -
Frequency MAF <0.01
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.66864 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 ?/. 3 c.596A>G r.(?) p.(His199Arg) -


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