Variant #0001302006 (NC_000014.8:g.20020068_20020069insTCG, NM_001145442.1:c.152_153insCGA (POTEM))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.20020068_20020069insTCG
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID POTEM_000002
Frequency 97/4386
Freq. EA 53/2836
Freq. AA 44/1550
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 2014-05-26 10:35:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
POTEM NM_001145442.1 ?/? c.152_153insCGA r.(?) p.(Asp51dup)