Variant #0001133226 (NC_000011.9:g.89018126A>G, NC_000011.9(NM_000372.4):c.1366+4A>G (TYR))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.89018126A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TYR_000094
Frequency 26/12994
Freq. EA 23/8592
Freq. AA 3/4402
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 2013-05-05 00:04:57 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TYR NM_000372.4 ?/? c.1366+4A>G r.spl? p.?