Variant #0000714690 (NC_000007.13:g.208992_208993insG, NC_000007.13(NM_020223.3):c.863+16_863+17insG (FAM20C))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.208992_208993insG
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FAM20C_000024
Frequency 2/11876
Freq. EA 2/7980
Freq. AA 0/3896
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 2014-06-15 21:42:04 +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.863+16_863+17insG r.(=) p.(=)