Variant #0009456123 (NC_000015.9:g.89659668G>A, NM_007011.7:c.110G>A (ABHD2))

Chromosome 15
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.89659668G>A
DB-ID -
dbSNP ID rs765530856
gnomAD frequency 1/246058
gnomAD homozygote count 0/123028
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     
ABHD2 NM_007011.7 ./. c.110G>A r.(?) p.(Ser37Asn)
ABHD2 NM_152924.4 ./. c.110G>A r.(?) p.(Ser37Asn)