Variant #0000200384 (NC_000002.11:g.41686T>C, NC_000002.11(NM_001077710.2):c.947-59A>G (FAM110C))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.41686T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FAM110C_000005
Frequency 11/4566
Freq. EA 0/3182
Freq. AA 11/1384
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 2014-04-19 16:45:43 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FAM110C NM_001077710.2 ?/? c.947-59A>G r.(=) p.(=)