Variant #0000714695 (NC_000007.13:g.286399G>C, NM_020223.3:c.882G>C (FAM20C))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.286399G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FAM20C_000029
Frequency 1/4566
Freq. EA 1/3182
Freq. AA 0/1384
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 16:28:58 +02:00 (CEST)
Date last edited 2014-05-05 01:40:25 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FAM20C NM_020223.3 ?/? c.882G>C r.(?) p.(Glu294Asp)