Variant #0000168256 (NC_000017.10:g.78086727C>G, NM_000152.3:c.1941C>G (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.78086727C>G
DNA change (hg38) g.80112928C>G
Published as -
ISCN -
DB-ID GAA_000034 See all 11 reported entries
Variant remarks predicted potentially less severe, classic infantile phenotype when combined with null allele; predicted CRIM+ (protein expressed); Align GVGD class C15 (GV: 195.00-GD: 116.53), SIFT deleterious (score: 0), Mutation Taster disease causing (p-value: 1)
Reference Pompe disease database 939
ClinVar ID -
dbSNP ID rs776948121
Origin SUMMARY record
Segregation -
Frequency MAF <0.01
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 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 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 +?/. 14 c.1941C>G r.(?) p.(Cys647Trp) -


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