Variant #0001852356 (NC_000020.10:g.42315629C>T, NM_002466.2:c.417C>T (MYBL2))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.42315629C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MYBL2_000033
Frequency 4/13006
Freq. EA 3/8600
Freq. AA 1/4406
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 16:46:43 +02:00 (CEST)
Date last edited 2013-05-06 04:56:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MYBL2 NM_002466.2 ?/? c.417C>T r.(=) p.(=)