Variant #0000168280 (NC_000017.10:g.78084529T>C, NM_000152.3:c.1441T>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.78084529T>C
DNA change (hg38) g.80110730T>C
Published as -
ISCN -
DB-ID GAA_000080 See all 5 reported entries
Variant remarks predicted potentially less severe, classic infantile phenotype when combined with null allele; predicted CRIM+ (protein expressed); Align GVGD class C65 (GV: 0.00-GD: 101.29), SIFT deleterious (score: 0), Mutation Taster disease causing (p-value: 1)
Reference Pompe disease database 805
ClinVar ID -
dbSNP ID rs772883420
Origin SUMMARY record
Segregation -
Frequency MAF <0.01
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-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 2025-03-11 20:08:49 +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 +?/. 10 c.1441T>C r.(?) p.(Trp481Arg) -


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