Variant #0001301982 (NC_000014.8:g.19559038T>C, NM_001005356.2:c.684T>C (POTEG))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.19559038T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID POTEG_000026
Frequency 1/11372
Freq. EA 1/7664
Freq. AA 0/3708
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 16:41:19 +02:00 (CEST)
Date last edited 2014-04-28 06:11:56 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
POTEG NM_001005356.2 ?/? c.684T>C r.(=) p.(=)