Variant #0000714698 (NC_000007.13:g.286512C>T, NC_000007.13(NM_020223.3):c.956+39C>T (FAM20C))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.286512C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FAM20C_000032
Frequency 6/4566
Freq. EA 0/3182
Freq. AA 6/1384
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 13:55:41 +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.956+39C>T r.(=) p.(=)