Variant #0000245339 (NC_000002.11:g.74754436G>C, NM_181575.3:c.1016C>G (AUP1))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.74754436G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AUP1_000018
Frequency 1/12196
Freq. EA 1/8282
Freq. AA 0/3914
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 22:45:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AUP1 NM_181575.3 ?/? c.1016C>G r.(?) p.(Ala339Gly)