Variant #0008670728 (NC_000014.8:g.23067229T>C, NM_022060.2:c.14T>C (ABHD4))

Chromosome 14
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.23067229T>C
DB-ID -
dbSNP ID -
gnomAD frequency 1/148840
gnomAD homozygote count 0/74419
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     
ABHD4 NM_022060.2 ./. c.14T>C r.(?) p.(Leu5Pro)