Variant #0010950268 (NC_000018.9:g.166774G>C, NC_000018.9(NM_005151.3):c.163-13G>C (USP14))

Chromosome 18
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.166774G>C
DB-ID -
dbSNP ID rs549895189
gnomAD frequency 3/245732
gnomAD homozygote count 0/122863
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     
USP14 NM_001037334.1 ./. c.163-13G>C r.(=) p.(=)
USP14 NM_005151.3 ./. c.163-13G>C r.(=) p.(=)