Variant #0001566179 (NC_000017.10:g.18220859T>C, NM_144775.2:c.1756T>C (SMCR8))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.18220859T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SMCR8_000074
Frequency 2/13006
Freq. EA 0/8600
Freq. AA 2/4406
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 16:44:12 +02:00 (CEST)
Date last edited 2013-05-05 16:39:27 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SMCR8 NM_144775.2 ?/? c.1756T>C r.(?) p.(Cys586Arg)