Variant #0001296040 (NC_000013.10:g.108881612A>G, NM_032859.2:c.46A>G (ABHD13))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.108881612A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD13_000002
Frequency 4/13004
Freq. EA 0/8598
Freq. AA 4/4406
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 2024-04-26 20:18:59 +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.46A>G r.(?) p.(Ile16Val)