Variant #0010906970 (NC_000017.10:g.79108236C>T, NM_001080395.2:c.121G>A (AATK))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.79108236C>T
DB-ID -
dbSNP ID rs779486236
gnomAD frequency 3/244762
gnomAD homozygote count 0/122378
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_001080395.2 ./. c.121G>A r.(?) p.(Gly41Arg)
AATK NM_004920.2 ./. c.-2655G>A r.(=) p.(=)