Variant #0001076069 (NC_000011.9:g.31815167A>T, NC_000011.9(NM_001604.4):c.958+33T>A (PAX6))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.31815167A>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PAX6_000016
Frequency 444/13002
Freq. EA 5/8598
Freq. AA 439/4404
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 2013-05-04 22:11:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PAX6 NM_001604.4 ?/? c.958+33T>A r.(=) p.(=)