Variant #0001408798 (NC_000002.11:g.27346865T>C, NM_032604.3:c.49T>C (ABHD1))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.27346865T>C
DB-ID -
dbSNP ID rs773421825
gnomAD frequency 1/246232
gnomAD homozygote count 0/123104
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CGREF1 NM_001166240.1 ./. c.-5163A>G r.(=) p.(=)
CGREF1 NM_006569.5 ./. c.-5163A>G r.(=) p.(=)
ABHD1 NM_032604.3 ./. c.49T>C r.(?) p.(Phe17Leu)