Variant #0010906999 (NC_000017.10:g.79108318T>A, NC_000017.10(NM_001080395.2):c.56-17A>T (AATK))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.79108318T>A
DB-ID -
dbSNP ID rs11658145
gnomAD frequency 4/227590
gnomAD homozygote count 0/68005
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.56-17A>T r.(=) p.(=)
AATK NM_004920.2 ./. c.-2737A>T r.(=) p.(=)