Variant #0000245372 (NC_000002.11:g.74755575_74755576insT, NM_181575.3:c.565_566insA (AUP1))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.74755575_74755576insT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AUP1_000048
Frequency 1/11562
Freq. EA 1/7890
Freq. AA 0/3672
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 22:45:34 +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.565_566insA r.(?) p.(Thr189Asnfs*50)