Variant #0010852708 (NC_000017.10:g.74448797_74448798insAA, NC_000017.10(NM_022066.3):c.417+9_417+10insTT (UBE2O))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74448797_74448798insAA
DB-ID -
dbSNP ID rs759558089
gnomAD frequency 1/42130
gnomAD homozygote count 0/21064
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.-1643_-1642insAA r.(=) p.(=)
UBE2O NM_022066.3 ./. c.417+9_417+10insTT r.(=) p.(=)