Variant #0000496952 (NC_000004.11:g.88903899C>T, NM_000582.2:c.754C>T (SPP1))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.88903899C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SPP1_000070
Frequency 16/13006
Freq. EA 16/8600
Freq. AA 0/4406
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 16:25:12 +02:00 (CEST)
Date last edited 2013-05-04 05:16:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SPP1 NM_000582.2 ?/? c.754C>T r.(?) p.(Leu252Phe)