Variant #0012146188 (NC_000020.10:g.25319953G>C, NM_015600.4:c.226C>G (ABHD12))

Chromosome 20
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.25319953G>C
DB-ID -
dbSNP ID rs751917613
gnomAD frequency 1/246192
gnomAD homozygote count 0/123095
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     
ABHD12 NM_001042472.2 ./. c.226C>G r.(?) p.(Leu76Val)
ABHD12 NM_015600.4 ./. c.226C>G r.(?) p.(Leu76Val)