Variant #0000200382 (NC_000002.11:g.41627del, NM_001077710.2:c.947del (FAM110C))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.41627del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FAM110C_000003
Frequency 1/11390
Freq. EA 1/7826
Freq. AA 0/3564
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 2014-06-12 11:00:22 +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.947del r.(?) p.(Gly316Glufs*30)