Variant #0012146152 (NC_000020.10:g.25304111A>G, NM_015600.4:c.317-45delTinsC (ABHD12))

Chromosome 20
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.25304111A>G
DB-ID -
dbSNP ID rs76752183
gnomAD frequency 1336/245438
gnomAD homozygote count 43/121423
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     
ABHD12 NM_001042472.2 ./. c.317-45delTinsC r.(=) p.(=)
ABHD12 NM_015600.4 ./. c.317-45delTinsC r.(=) p.(=)