Variant #0012146195 (NC_000020.10:g.25319977C>T, NM_015600.4:c.202G>A (ABHD12))

Chromosome 20
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.25319977C>T
DB-ID -
dbSNP ID rs11904930
gnomAD frequency 429/246206
gnomAD homozygote count 7/122681
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     
ABHD12 NM_001042472.2 ./. c.202G>A r.(?) p.(Val68Met)
ABHD12 NM_015600.4 ./. c.202G>A r.(?) p.(Val68Met)