Variant #0001296045 (NC_000013.10:g.108881858C>T, NM_032859.2:c.292C>T (ABHD13))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.108881858C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD13_000007
Frequency 6/13002
Freq. EA 5/8596
Freq. AA 1/4406
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 16:41:01 +02:00 (CEST)
Date last edited 2018-09-30 11:43:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD13 NM_032859.2 ?/? c.292C>T r.(?) p.(Arg98Cys)