Variant #0000245386 (NC_000002.11:g.74756112_74756113insAA, NC_000002.11(NM_181575.3):c.340-51_340-50insTT (AUP1))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.74756112_74756113insAA
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AUP1_000064
Frequency 202/11358
Freq. EA 55/7820
Freq. AA 147/3538
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 22:45:35 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AUP1 NM_181575.3 ?/? c.340-51_340-50insTT r.(=) p.(=)