Variant #0001794513 (NC_000019.9:g.50173424_50173425insG, NC_000019.9(NM_001040668.1):c.679-49_679-48insG (BCL2L12))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.50173424_50173425insG
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL2L12_000045
Frequency 733/9890
Freq. EA 463/6662
Freq. AA 270/3228
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 16:45:39 +02:00 (CEST)
Date last edited 2013-05-06 02:23:16 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L12 NM_001040668.1 ?/? c.679-49_679-48insG r.(=) p.(=)