Variant #0008781299 (NC_000014.8:g.51347331G>C, NC_000014.8(NM_001206673.1):c.455+42G>C (ABHD12B))

Chromosome 14
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.51347331G>C
DB-ID -
dbSNP ID rs776694397
gnomAD frequency 3/182794
gnomAD homozygote count 0/91394
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+42G>C r.(=) p.(=)
ABHD12B NM_181814.1 ./. c.224+42G>C r.(=) p.(=)