Variant #0000200404 (NC_000002.11:g.45953T>C, NM_001077710.2:c.433A>G (FAM110C))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.45953T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FAM110C_000025
Frequency 20/11630
Freq. EA 18/8022
Freq. AA 2/3608
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 2014-03-28 23:28:37 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FAM110C NM_001077710.2 ?/? c.433A>G r.(?) p.(Lys145Glu)