Variant #0004253556 (NC_000006.11:g.31675895C>G, NM_021160.2:c.-4837G>C (ABHD16A))

Chromosome 6
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.31675895C>G
DB-ID -
dbSNP ID rs746440871
gnomAD frequency 1/194536
gnomAD homozygote count 0/97267
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
LY6G6F NM_001003693.1 ./. c.630C>G r.(?) p.(Val210=)
ABHD16A NM_021160.2 ./. c.-4837G>C r.(=) p.(=)