Variant #0000714680 (NC_000007.13:g.195681G>A, NM_020223.3:c.733G>A (FAM20C))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.195681G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FAM20C_000014
Frequency 24/12612
Freq. EA 0/8414
Freq. AA 24/4198
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 13:55:27 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FAM20C NM_020223.3 ?/? c.733G>A r.(?) p.(Ala245Thr)