Variant #0000168281 (NC_000017.10:g.78090814G>C, NM_000152.3:c.2237G>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.78090814G>C
DNA change (hg38) g.80117015G>C
Published as -
ISCN -
DB-ID GAA_000225 See all 3 reported entries
Variant remarks predicted potentially less severe, childhood phenotype when combined with null allele; predicted CRIM+ (protein expressed); Align GVGD class C0 (GV: 268.54-GD: 61.50), SIFT deleterious (score: 0), Mutation Taster disease causing (p-value: 1)
Reference Pompe disease database 997
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency MAF not reported
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 6.0E-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 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 +?/. 16 c.2237G>C r.(?) p.(Trp746Ser) 0.1% residual activity, affects secretion & processing in expression study


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