Variant #0004999662 (NC_000007.13:g.73152796G>A, NC_000007.13(NM_148912.2):c.153-3C>T (ABHD11))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.73152796G>A
DB-ID -
dbSNP ID rs150117672
gnomAD frequency 2449/231406
gnomAD homozygote count 24/113278
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     
ABHD11 NM_001145364.1 ./. c.153-3C>T r.spl? p.?
ABHD11 NM_148912.2 ./. c.153-3C>T r.spl? p.?
ABHD11 NM_148913.2 ./. c.153-24C>T r.(=) p.(=)