Variant #0000487433 (NC_000017.10:g.78078931G>T, NM_000152.3:c.546G>T (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.78078931G>T
DNA change (hg38) g.80105132G>T
Published as -
ISCN -
DB-ID GAA_000466 See all 8 reported entries
Variant remarks functional analysis using expression cloning in minigene splicing assay; complete skipping of exon 2
Reference Dardis 2019, submitted
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Andrea Elena Dardis
Database submission license No license selected
Created by Andrea Elena Dardis
Date created 2019-06-14 14:34:52 +02:00 (CEST)
Date last edited 2019-07-08 15:36:28 +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 +/. 2 c.546G>T r.-32_546del p.0? -


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