Variant #0005728256 (NC_000008.10:g.117950726_117950727insAGGCGGCGG, NM_001025357.2:c.244_245insAGGCGGCGG (AARD))

Chromosome 8
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.117950726_117950727insAGGCGGCGG
DB-ID -
dbSNP ID rs777722026
gnomAD frequency 8/146382
gnomAD homozygote count 0/72594
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AARD NM_001025357.2 ./. c.244_245insAGGCGGCGG r.(?) p.(Glu81_Ala82insGluAlaAla)