Variant #0000000498 (NC_000001.10:g.874665G>A, NM_152486.2:c.531G>A (SAMD11))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.874665G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SAMD11_000071
Frequency 197/12950
Freq. EA 5/8576
Freq. AA 192/4374
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 2015-07-30 09:02:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SAMD11 NM_152486.2 ?/? c.531G>A r.(=) p.(=)