Variant #0001296042 (NC_000013.10:g.108881686T>C, NM_032859.2:c.120T>C (ABHD13))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.108881686T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD13_000004
Frequency 1/13004
Freq. EA 0/8598
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 11:42:03 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD13 NM_032859.2 ?/? c.120T>C r.(=) p.(=)