Variant #0001566172 (NC_000017.10:g.18220770G>A, NM_144775.2:c.1667G>A (SMCR8))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.18220770G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SMCR8_000067
Frequency 9529/13006
Freq. EA 5804/8600
Freq. AA 3725/4406
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 16:39:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SMCR8 NM_144775.2 ?/? c.1667G>A r.(?) p.(Arg556His)