Variant #0001581336 (NC_000017.10:g.35310195T>C, NM_012138.3:c.293T>C (AATF))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.35310195T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AATF_000018
Frequency 160/13006
Freq. EA 0/8600
Freq. AA 160/4406
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 2018-08-22 23:46:16 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AATF NM_012138.3 ?/? c.293T>C r.(?) p.(Ile98Thr)