Variant #0000200380 (NC_000002.11:g.41612C>T, NM_001077710.2:c.962G>A (FAM110C))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.41612C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FAM110C_000001
Frequency 2/11882
Freq. EA 1/8178
Freq. AA 1/3704
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 2014-05-04 16:40:32 +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.962G>A r.(?) p.(Arg321Gln)