Variant #0001837654 (NC_000020.10:g.25288692A>C, NC_000020.10(NM_015600.4):c.788-11T>G (ABHD12))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.25288692A>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD12_000041
Frequency 4/13006
Freq. EA 0/8600
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 16:46:43 +02:00 (CEST)
Date last edited 2024-12-24 11:27:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD12 NM_015600.4 ?/? c.788-11T>G r.(=) p.(=)