Variant #0005728168 (NC_000008.10:g.117950436C>T, NM_001025357.2:c.-47C>T (AARD))

Chromosome 8
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.117950436C>T
DB-ID -
dbSNP ID rs750852349
gnomAD frequency 1/164528
gnomAD homozygote count 0/82263
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.-47C>T r.(=) p.(=)