Variant #0000000444 (NC_000001.10:g.865700C>T, NM_152486.2:c.238C>T (SAMD11))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.865700C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SAMD11_000017
Frequency 14/12978
Freq. EA 0/8592
Freq. AA 14/4386
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 2014-04-28 21:05:26 +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.238C>T r.(?) p.(Arg80Cys)