Variant #0010852722 (NC_000017.10:g.74449130G>A, NM_022066.3:c.94C>T (UBE2O))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74449130G>A
DB-ID -
dbSNP ID rs552502199
gnomAD frequency 16/30846
gnomAD homozygote count 0/15407
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.-1310G>A r.(=) p.(=)
UBE2O NM_022066.3 ./. c.94C>T r.(?) p.(Pro32Ser)