Variant #0000168289 (NC_000017.10:g.78078341T>G, NC_000017.10(NM_000152.3):c.-32-13T>G (GAA))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.78078341T>G
DNA change (hg38) g.80104542T>G
Published as -
ISCN -
DB-ID GAA_000029 See all 345 reported entries
Variant remarks predicted potentially mild, childhood/adult phenotype when combined with null allele; predicted CRIM+ (leaky normal splicing)
Reference Pompe disease database 568
ClinVar ID -
dbSNP ID rs386834236
Origin SUMMARY record
Segregation -
Frequency MAF <0.01
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00347 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 2022-12-17 19:36:12 +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 +/. 1i c.-32-13T>G r.[=,-32_546del,-32_486del] p.[=,0] -


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