Variant #0012368532 (NC_000020.10:g.62489056G>C, NM_080622.3:c.-3838G>C (ABHD16B))

Chromosome 20
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.62489056G>C
DB-ID -
dbSNP ID rs560260131
gnomAD frequency 11/193310
gnomAD homozygote count 0/96644
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     
ABHD16B NM_080622.3 ./. c.-3838G>C r.(=) p.(=)