Variant #0000985913 (NC_000010.10:g.45920617_45920620del, NC_000010.10(NM_000698.3):c.834+37_834+40del (ALOX5))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.45920617_45920620del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ALOX5_000067
Frequency 2/12516
Freq. EA 0/8254
Freq. AA 2/4262
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 16:30:47 +02:00 (CEST)
Date last edited 2013-05-04 19:16:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ALOX5 NM_000698.3 ?/? c.834+37_834+40del r.(=) p.(=)