Variant #0001133196 (NC_000011.9:g.88925183G>A, NC_000011.9(NM_000372.4):c.1036+597G>A (TYR))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.88925183G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TYR_000065
Frequency 1/5626
Freq. EA 1/3914
Freq. AA 0/1712
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 2013-05-05 00:04:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TYR NM_000372.4 ?/? c.1036+597G>A r.(=) p.(=)