Variant #0012146198 (NC_000020.10:g.25319986G>A, NM_015600.4:c.193C>T (ABHD12))

Chromosome 20
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.25319986G>A
DB-ID -
dbSNP ID rs758316679
gnomAD frequency 5/246204
gnomAD homozygote count 0/123097
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.193C>T r.(?) p.(Arg65Ter)
ABHD12 NM_015600.4 ./. c.193C>T r.(?) p.(Arg65Ter)