Variant #0004999738 (NC_000007.13:g.73153119G>C, NM_148912.2:c.9C>G (ABHD11))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.73153119G>C
DB-ID -
dbSNP ID rs782557629
gnomAD frequency 6/225188
gnomAD homozygote count 0/112587
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.9C>G r.(?) p.(Ala3=)
ABHD11 NM_148912.2 ./. c.9C>G r.(?) p.(Ala3=)
ABHD11 NM_148913.2 ./. c.9C>G r.(?) p.(Ala3=)