Variant #0000714708 (NC_000007.13:g.295960T>A, NM_020223.3:c.1218T>A (FAM20C))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.295960T>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FAM20C_000042
Frequency 132/4566
Freq. EA 87/3182
Freq. AA 45/1384
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 2014-05-04 17:20:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FAM20C NM_020223.3 ?/? c.1218T>A r.(=) p.(=)