Variant #0008781142 (NC_000014.8:g.51338991C>T, NM_001206673.1:c.99C>T (ABHD12B))

Chromosome 14
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.51338991C>T
DB-ID -
dbSNP ID rs190024469
gnomAD frequency 13/39710
gnomAD homozygote count 0/19842
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD12B NM_001206673.1 ./. c.99C>T r.(?) p.(Asn33=)
ABHD12B NM_181814.1 ./. c.99C>T r.(?) p.(Asn33=)