Variant #0000180882 (NC_000001.10:g.223998136G>A, NM_001031685.2:c.369C>T (TP53BP2))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.223998136G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TP53BP2_000154
Frequency 15/11776
Freq. EA 13/8146
Freq. AA 2/3630
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 16:20:35 +02:00 (CEST)
Date last edited 2013-05-03 21:03:59 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TP53BP2 NM_001031685.2 ?/? c.369C>T r.(=) p.(=)