Variant #0001852342 (NC_000020.10:g.42311379G>T, NC_000020.10(NM_002466.2):c.187-55G>T (MYBL2))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.42311379G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MYBL2_000019
Frequency 1/4566
Freq. EA 1/3182
Freq. AA 0/1384
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 04:56:57 +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.187-55G>T r.(=) p.(=)