Variant #0001408828 (NC_000002.11:g.27346942T>C, NC_000002.11(NM_032604.3):c.114+12T>C (ABHD1))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.27346942T>C
DB-ID -
dbSNP ID rs774334737
gnomAD frequency 1/245974
gnomAD homozygote count 0/122986
Average frequency (gnomAD v.2.1.1) 0 View details
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     
CGREF1 NM_001166240.1 ./. c.-5240A>G r.(=) p.(=)
CGREF1 NM_006569.5 ./. c.-5240A>G r.(=) p.(=)
ABHD1 NM_032604.3 ./. c.114+12T>C r.(=) p.(=)