Variant #0007900149 (NC_000012.11:g.40013159G>C, NM_005164.3:c.259C>G (ABCD2))

Chromosome 12
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.40013159G>C
DB-ID -
dbSNP ID rs762731548
gnomAD frequency 7/246242
gnomAD homozygote count 0/123114
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     
ABCD2 NM_005164.3 ./. c.259C>G r.(?) p.(Gln87Glu)