Variant #0004999658 (NC_000007.13:g.73152767A>G, NM_148912.2:c.179T>C (ABHD11))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.73152767A>G
DB-ID -
dbSNP ID rs781989831
gnomAD frequency 8/235388
gnomAD homozygote count 0/117686
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.179T>C r.(?) p.(Leu60Pro)
ABHD11 NM_148912.2 ./. c.179T>C r.(?) p.(Leu60Pro)
ABHD11 NM_148913.2 ./. c.158T>C r.(?) p.(Leu53Pro)