Variant #0000200406 (NC_000002.11:g.46037C>T, NM_001077710.2:c.349G>A (FAM110C))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.46037C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FAM110C_000027
Frequency 1/11958
Freq. EA 0/8166
Freq. AA 1/3792
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 04:25:59 +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.349G>A r.(?) p.(Gly117Ser)