Variant #0010906923 (NC_000017.10:g.79107185A>C, NM_004920.2:c.-1604T>G (AATK))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.79107185A>C
DB-ID -
dbSNP ID rs773861693
gnomAD frequency 2/41742
gnomAD homozygote count 0/20869
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     
AATK NM_004920.2 ./. c.-1604T>G r.(=) p.(=)