Variant #0001141305 (NC_000011.9:g.108098576C>G, NM_000051.3:c.146C>G (ATM))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.108098576C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ATM_000011
Frequency 129/12990
Freq. EA 117/8588
Freq. AA 12/4402
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 16:37:25 +02:00 (CEST)
Date last edited 2017-01-03 23:57:47 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ATM NM_000051.3 ?/? c.146C>G r.(?) p.(Ser49Cys)