Variant #0000478291 (NC_000017.10:g.78084525G>C, NC_000017.10(NM_000152.3):c.1438-1G>C (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.78084525G>C
DNA change (hg38) g.80110726G>C
Published as -
ISCN -
DB-ID GAA_000096 See all 4 reported entries
Variant remarks predicted very severe, unknown (disease-associated) phenotype when combined with null allele; predicted CRIM? (protein expression unknown)
Reference Pompe disease database 802
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 Pim Pijnappel
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-05-09 16:06:10 +02:00 (CEST)
Date last edited 2020-07-14 14:26:09 +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 +/. 9i c.1438-1G>C r.spl p.? -


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