Variant #0001296063 (NC_000013.10:g.108882599T>C, NM_032859.2:c.*19T>C (ABHD13))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.108882599T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD13_000025
Frequency 1/12978
Freq. EA 1/8586
Freq. AA 0/4392
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 11:47:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD13 NM_032859.2 ?/? c.*19T>C r.(=) p.(=)