Variant #0011193569 (NC_000019.9:g.1881488G>A, NM_031213.3:c.78C>T (ABHD17A))

Chromosome 19
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.1881488G>A
DB-ID -
dbSNP ID rs200425255
gnomAD frequency 549/230172
gnomAD homozygote count 3/114540
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     
ABHD17A NM_001130111.1 ./. c.78C>T r.(?) p.(Leu26=)
ABHD17A NM_031213.3 ./. c.78C>T r.(?) p.(Leu26=)