Variant #0000478311 (NC_000017.10:g.78084773_78084774delinsGT, NM_000152.3:c.1585_1586delinsGT (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.78084773_78084774delinsGT
DNA change (hg38) g.80110974_80110975delinsGT
Published as 1585_1586TC>GT
ISCN -
DB-ID GAA_000054 See all 6 reported entries
Variant remarks predicted potentially mild, adult phenotype when combined with null allele; predicted CRIM+ (protein expressed)
Reference Pompe disease database 847
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 2019-06-28 11:29:39 +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 +?/. 11 c.1585_1586delinsGT r.(?) p.(Ser529Val) -


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