Variant #0001644308 (NC_000017.10:g.79107083C>T, NC_000017.10(NM_004920.2):c.-1502G>A (AATK))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.79107083C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AATK_000214
Frequency 1/12360
Freq. EA 1/8322
Freq. AA 0/4038
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:44:12 +02:00 (CEST)
Date last edited 2018-08-23 05:20:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AATK NM_004920.2 ?/? c.-1502G>A N/A N/A
MIR1250 NR_031652.1 ?/? n.26G>A N/A N/A