Variant #0001581409 (NC_000017.10:g.35348176_35348177del, NC_000017.10(NM_012138.3):c.1398+20_1398+21del (AATF))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.35348176_35348177del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AATF_000091
Frequency 1/12518
Freq. EA 0/8254
Freq. AA 1/4264
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 04:35:01 +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.1398+20_1398+21del r.(=) p.(=)