Variant #0000164199 (NC_000017.10:g.78090880C>G, NM_000152.3:c.2303C>G (GAA))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.78090880C>G
DNA change (hg38) g.80117081C>G
Published as P768R
ISCN -
DB-ID GAA_000049 See all 5 reported entries
Variant remarks COS cell cDNA expression cloning shows no lysosomal alpha-glucosidase activity, severely impaired GAA-protein maturation and no secretion
Reference PubMed: Hermans 1998
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-03-18 19:24:13 +01:00 (CET)
Date last edited 2020-07-14 21:55:22 +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.2303C>G r.(?) p.Pro768Arg -


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