Variant #0001573816 (NC_000017.10:g.27890144G>C, NC_000017.10(NM_198147.2):c.882-40C>G (ABHD15))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.27890144G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD15_000042
Frequency 128/12414
Freq. EA 1/8232
Freq. AA 127/4182
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 16:44:12 +02:00 (CEST)
Date last edited 2018-08-23 09:40:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD15 NM_198147.2 ?/? c.882-40C>G r.(=) p.(=)