Variant #0004253528 (NC_000006.11:g.31675762T>G, NM_021160.2:c.-4704A>C (ABHD16A))

Chromosome 6
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.31675762T>G
DB-ID -
dbSNP ID rs570757958
gnomAD frequency 2/241154
gnomAD homozygote count 0/120575
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     
LY6G6F NM_001003693.1 ./. c.497T>G r.(?) p.(Val166Gly)
ABHD16A NM_001177515.1 ./. c.-5217A>C r.(=) p.(=)
ABHD16A NM_021160.2 ./. c.-4704A>C r.(=) p.(=)