Variant #0000482477 (NC_000004.11:g.57244496_57244497del, NM_181806.2:c.485_486del (AASDH))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.57244496_57244497del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AASDH_000152
Frequency 1/12520
Freq. EA 0/8254
Freq. AA 1/4266
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 16:25:12 +02:00 (CEST)
Date last edited 2018-08-23 03:42:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AASDH NM_181806.2 ?/? c.485_486del r.(?) p.(Tyr162*)