Variant #0000288096 (NC_000017.10:g.78078643dup, NM_000152.3:c.258dup (GAA))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.78078643dup
DNA change (hg38) g.80104844dup
Published as GAA(NM_000152.3):c.258dupC (p.N87Qfs*9), GAA(NM_000152.5):c.258dupC (p.N87Qfs*9)
ISCN -
DB-ID GAA_000060 See all 14 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Enzyme activity     
GAA NM_000152.3 +/. - c.258dup r.(?) p.(Asn87GlnfsTer9) -
CCDC40 NM_017950.3 +/. - c.*5069dup r.(?) p.(=) -


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