Variant #0000168318 (NC_000017.10:g.78091658_78092195del, NC_000017.10(NM_000152.3):c.2481+110_2646+39del (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.78091658_78092195del
DNA change (hg38) g.80117859_80118396del
Published as -
ISCN -
DB-ID GAA_000037 See all 34 reported entries
Variant remarks predicted very severe, classic infantile phenotype when combined with null allele; predicted CRIM+ (endogenous protein on Western blot)
Reference Pompe disease database 1039
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency MAF not reported
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 2025-06-08 07:34:00 +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 +/. 17i c.2481+110_2646+39del r.2482_2646del p.(Gly828_Asn882del) -


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