Variant #0000637931 (NC_000006.11:g.31657448T>C, NM_001177515.1:c.892A>G (ABHD16A))

Chromosome 6
DNA change (genomic) (Relative to hg19 / GRCh37) g.31657448T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD16A_000042
Frequency 1/8438
Freq. EA 1/5416
Freq. AA 0/3022
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 16:27:59 +02:00 (CEST)
Date last edited 2018-08-23 02:22:02 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD16A NM_001177515.1 ?/? c.892A>G r.(?) p.(Met298Val)