Variant #0000000504 (NC_000001.10:g.874748T>C, NM_152486.2:c.614T>C (SAMD11))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.874748T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SAMD11_000077
Frequency 1/13002
Freq. EA 1/8600
Freq. AA 0/4402
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 2014-02-26 19:09:47 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SAMD11 NM_152486.2 ?/? c.614T>C r.(?) p.(Phe205Ser)