Variant #0001133216 (NC_000011.9:g.89017961G>A, NM_000372.4:c.1205G>A (TYR))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.89017961G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TYR_000080
Frequency 2641/13000
Freq. EA 2418/8598
Freq. AA 223/4402
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 16:37:25 +02:00 (CEST)
Date last edited 2013-12-23 19:01:47 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TYR NM_000372.4 ?/? c.1205G>A r.(?) p.(Arg402Gln)