Variant #0008606299 (NC_000013.10:g.108881792C>G, NM_032859.2:c.226C>G (ABHD13))

Chromosome 13
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.108881792C>G
DB-ID -
dbSNP ID rs749374616
gnomAD frequency 2/245360
gnomAD homozygote count 0/122678
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     
ABHD13 NM_032859.2 ./. c.226C>G r.(?) p.(Leu76Val)