Variant #0000886049 (NC_000009.11:g.12694063C>T, NM_000550.2:c.67C>T (TYRP1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.12694063C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TYRP1_000005
Frequency 5/13006
Freq. EA 3/8600
Freq. AA 2/4406
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 16:29:58 +02:00 (CEST)
Date last edited 2013-05-04 16:14:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TYRP1 NM_000550.2 ?/? c.67C>T r.(?) p.(Arg23Trp)