Variant #0000200393 (NC_000002.11:g.45610C>T, NM_001077710.2:c.776G>A (FAM110C))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.45610C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FAM110C_000014
Frequency 1/12558
Freq. EA 1/8408
Freq. AA 0/4150
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 2014-04-28 15:20:40 +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.776G>A r.(?) p.(Gly259Asp)