Variant #0000180896 (NC_000001.10:g.224009123A>G, NC_000001.10(NM_001031685.2):c.28-54T>C (TP53BP2))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.224009123A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TP53BP2_000165
Frequency 2/5734
Freq. EA 0/3982
Freq. AA 2/1752
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 21:04:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TP53BP2 NM_001031685.2 ?/? c.28-54T>C r.(=) p.(=)