Variant #0001076119 (NC_000011.9:g.31827998C>T, NM_001604.4:c.-39G>A (PAX6))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.31827998C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PAX6_000066
Frequency 1/12992
Freq. EA 0/8590
Freq. AA 1/4402
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 2013-05-04 22:11:58 +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.-39G>A r.(=) p.(=)