Variant #0011004689 (NC_000018.9:g.19231719G>C, NM_138340.4:c.1063delCinsG (ABHD3))

Chromosome 18
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.19231719G>C
DB-ID -
dbSNP ID rs774469085
gnomAD frequency 2/200120
gnomAD homozygote count 0/100057
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     
ABHD3 NM_138340.4 ./. c.1063delCinsG r.(?) p.(Pro355Ala)