Variant #0000168273 (NC_000017.10:g.78082197T>C, NM_000152.3:c.1064T>C (GAA))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.78082197T>C
DNA change (hg38) g.80108398T>C
Published as -
ISCN -
DB-ID GAA_000129 See all 18 reported entries
Variant remarks predicted potentially less severe, classic infantile/childhood phenotype when combined with null allele; predicted CRIM+ (endogenous protein on Western blot) ; Align GVGD class C0 (GV: 120.48-GD: 28.88), SIFT tolerated (score: 0.08), Mutation Taster disease causing (p-value: 1)
Reference Pompe disease database 715
ClinVar ID -
dbSNP ID rs766074609
Origin SUMMARY record
Segregation -
Frequency MAF <0.01
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-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 2025-03-15 10:41:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Enzyme activity     
GAA NM_000152.3 +?/. 6 c.1064T>C r.(?) p.(Leu355Pro) -


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