Variant #0001323950 (NC_000014.8:g.51370142A>G, NM_001206673.1:c.899A>G (ABHD12B))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.51370142A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD12B_000065
Frequency 10/13006
Freq. EA 2/8600
Freq. AA 8/4406
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 16:41:19 +02:00 (CEST)
Date last edited 2018-08-23 09:49:25 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD12B NM_001206673.1 ?/? c.899A>G r.(?) p.(His300Arg)