Variant #0008781288 (NC_000014.8:g.51347286A>G, NM_001206673.1:c.452A>G (ABHD12B))

Chromosome 14
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.51347286A>G
DB-ID -
dbSNP ID -
gnomAD frequency 0/222524
gnomAD homozygote count 0/111259
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     
ABHD12B NM_001206673.1 ./. c.452A>G r.(?) p.(His151Arg)
ABHD12B NM_181814.1 ./. c.221A>G r.(?) p.(His74Arg)