Variant #0000000488 (NC_000001.10:g.874456G>A, NM_152486.2:c.467G>A (SAMD11))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.874456G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SAMD11_000061
Frequency 17/13002
Freq. EA 1/8600
Freq. AA 16/4402
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 16:20:35 +02:00 (CEST)
Date last edited 2014-02-16 07:23:36 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SAMD11 NM_152486.2 ?/? c.467G>A r.(?) p.(Arg156His)