Variant #0000443126 (NC_000003.11:g.183905699G>T, NM_018358.2:c.497G>T (ABCF3))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.183905699G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCF3_000061
Frequency 1/13006
Freq. EA 0/8600
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 16:23:53 +02:00 (CEST)
Date last edited 2018-08-22 23:48:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCF3 NM_018358.2 ?/? c.497G>T r.(?) p.(Arg166Leu)