Variant #0010852716 (NC_000017.10:g.74449042A>T, NM_022066.3:c.182T>A (UBE2O))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74449042A>T
DB-ID -
dbSNP ID -
gnomAD frequency 1/95488
gnomAD homozygote count 0/47743
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AANAT NM_001166579.1 ./. c.-1398A>T r.(=) p.(=)
UBE2O NM_022066.3 ./. c.182T>A r.(?) p.(Phe61Tyr)