Variant #0001301970 (NC_000014.8:g.19553785C>T, NM_001005356.2:c.369C>T (POTEG))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.19553785C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID POTEG_000014
Frequency 1/12996
Freq. EA 0/8594
Freq. AA 1/4402
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 16:41:19 +02:00 (CEST)
Date last edited 2014-05-04 14:35:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
POTEG NM_001005356.2 ?/? c.369C>T r.(=) p.(=)