Variant #0000200391 (NC_000002.11:g.45580_45582del, NM_001077710.2:c.804_806del (FAM110C))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.45580_45582del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FAM110C_000012
Frequency 19/11836
Freq. EA 16/7958
Freq. AA 3/3878
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 16:22:05 +02:00 (CEST)
Date last edited 2014-06-14 04:10:27 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FAM110C NM_001077710.2 ?/? c.804_806del r.(?) p.(Asp268del)