Variant #0001900029 (NC_000022.10:g.16266920_16266921insAG, NC_000022.10(NM_001136213.1):c.1520+8_1520+9insCT (POTEH))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.16266920_16266921insAG
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID POTEH_000001
Frequency 1387/4398
Freq. EA 1018/3002
Freq. AA 369/1396
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 16:50:05 +02:00 (CEST)
Date last edited 2014-04-30 01:55:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
POTEH NM_001136213.1 ?/? c.1520+8_1520+9insCT r.(=) p.(=)