Variant #0009417194 (NC_000015.9:g.80988168A>C, NM_021214.1:c.398A>C (ABHD17C))

Chromosome 15
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.80988168A>C
DB-ID -
dbSNP ID rs755990261
gnomAD frequency 1/201484
gnomAD homozygote count 0/100741
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     
ABHD17C NM_021214.1 ./. c.398A>C r.(?) p.(Tyr133Ser)