Variant #0003481632 (NC_000004.11:g.171010868_171010869insCTTCTT, NM_016228.3:c.-28_-27insAAGAAG (AADAT))

Chromosome 4
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.171010868_171010869insCTTCTT
DB-ID -
dbSNP ID rs779902748
gnomAD frequency 1/245846
gnomAD homozygote count 0/122919
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AADAT NM_016228.3 ./. c.-28_-27insAAGAAG r.(=) p.(=)
AADAT NM_182662.1 ./. c.-28_-27insAAGAAG r.(=) p.(=)