Variant #0000496933 (NC_000004.11:g.88902991G>A, NC_000004.11(NM_000582.2):c.498+41G>A (SPP1))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.88902991G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SPP1_000044
Frequency 6/13006
Freq. EA 4/8600
Freq. AA 2/4406
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 05:16:27 +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.498+41G>A r.(=) p.(=)