Variant #0008606272 (NC_000013.10:g.108881639C>A, NM_032859.2:c.73C>A (ABHD13))

Chromosome 13
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.108881639C>A
DB-ID -
dbSNP ID rs147102037
gnomAD frequency 15/240708
gnomAD homozygote count 0/120339
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     
ABHD13 NM_032859.2 ./. c.73C>A r.(?) p.(Leu25Ile)