Variant #0008781139 (NC_000014.8:g.51338859G>T, NM_001206673.1:c.-34G>T (ABHD12B))

Chromosome 14
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.51338859G>T
DB-ID -
dbSNP ID rs566534033
gnomAD frequency 1/4830
gnomAD homozygote count 0/2413
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.-34G>T r.(=) p.(=)
ABHD12B NM_181814.1 ./. c.-34G>T r.(=) p.(=)