Variant #0000341157 (NC_000003.11:g.361508C>T, NM_006614.3:c.49C>T (CHL1))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.361508C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CHL1_000008
Frequency 4018/13004
Freq. EA 1740/8600
Freq. AA 2278/4404
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 16:23:53 +02:00 (CEST)
Date last edited 2014-05-04 16:20:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CHL1 NM_006614.3 ?/? c.49C>T r.(?) p.(Leu17Phe)