Variant #0010906957 (NC_000017.10:g.79108211A>G, NM_001080395.2:c.146T>C (AATK))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.79108211A>G
DB-ID -
dbSNP ID rs367712061
gnomAD frequency 1/244994
gnomAD homozygote count 0/122496
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.146T>C r.(?) p.(Met49Thr)
AATK NM_004920.2 ./. c.-2630T>C r.(=) p.(=)