Variant #0000886136 (NC_000009.11:g.12704606G>C, NM_000550.2:c.1162G>C (TYRP1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.12704606G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TYRP1_000092
Frequency 1/13006
Freq. EA 1/8600
Freq. AA 0/4406
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 16:14:51 +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.1162G>C r.(?) p.(Gly388Arg)