Variant #0001301999 (NC_000014.8:g.19571429T>C, NC_000014.8(NM_001005356.2):c.1197+11T>C (POTEG))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.19571429T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID POTEG_000043
Frequency 1/12336
Freq. EA 0/8138
Freq. AA 1/4198
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 20:10:59 +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.1197+11T>C r.(=) p.(=)