Variant #0008781295 (NC_000014.8:g.51347311T>A, NC_000014.8(NM_001206673.1):c.455+22T>A (ABHD12B))

Chromosome 14
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.51347311T>A
DB-ID -
dbSNP ID rs757947582
gnomAD frequency 4/162200
gnomAD homozygote count 0/80999
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     
ABHD12B NM_001206673.1 ./. c.455+22T>A r.(=) p.(=)
ABHD12B NM_181814.1 ./. c.224+22T>A r.(=) p.(=)