Variant #0000245363 (NC_000002.11:g.74755166G>A, NC_000002.11(NM_181575.3):c.672-33C>T (AUP1))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.74755166G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AUP1_000039
Frequency 1/12200
Freq. EA 1/8298
Freq. AA 0/3902
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 16:22:05 +02:00 (CEST)
Date last edited 2013-05-03 22:45:31 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AUP1 NM_181575.3 ?/? c.672-33C>T r.(=) p.(=)