Variant #0000183074 (NC_000001.10:g.227073271C>T, NM_000447.2:c.389C>T (PSEN2))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.227073271C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PSEN2_000046
Frequency 9/13006
Freq. EA 9/8600
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 16:20:35 +02:00 (CEST)
Date last edited 2014-07-07 20:50:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PSEN2 NM_000447.2 ?/? c.389C>T r.(?) p.(Ser130Leu)


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