Variant #0001581369 (NC_000017.10:g.35344041A>G, NC_000017.10(NM_012138.3):c.947+11A>G (AATF))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.35344041A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AATF_000051
Frequency 6/13006
Freq. EA 0/8600
Freq. AA 6/4406
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 2018-08-23 00:36:41 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AATF NM_012138.3 ?/? c.947+11A>G r.(=) p.(=)