Variant #0000245402 (NC_000002.11:g.74756532C>G, NM_181575.3:c.145G>C (AUP1))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.74756532C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID HTRA2_000001
Frequency 2/12768
Freq. EA 2/8486
Freq. AA 0/4282
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     
HTRA2 NM_013247.4 ?/? c.-602C>G r.(?) p.(Val49Leu)
AUP1 NM_181575.3 ?/? c.145G>C r.(?) p.(Val49Leu)