Variant #0000200395 (NC_000002.11:g.45622G>T, NM_001077710.2:c.764C>A (FAM110C))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.45622G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FAM110C_000016
Frequency 1/12698
Freq. EA 1/8464
Freq. AA 0/4234
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 05:35:48 +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.764C>A r.(?) p.(Thr255Asn)