Variant #0006020590 (NC_000009.11:g.74526886A>G, NM_001025780.1:c.-1340T>C (ABHD17B))

Chromosome 9
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74526886A>G
DB-ID -
dbSNP ID -
gnomAD frequency 1/179658
gnomAD homozygote count 0/89828
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     
ABHD17B NM_001025780.1 ./. c.-1340T>C r.(=) p.(=)
ABHD17B NM_016014.2 ./. c.-1340T>C r.(=) p.(=)