Variant #0002098461 (NC_000002.11:g.215896672T>C, NM_015657.3:c.-21A>G (ABCA12))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.215896672T>C
DB-ID -
dbSNP ID rs200465729
gnomAD frequency 261/242674
gnomAD homozygote count 1/121076
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     
ABCA12 NM_015657.3 ./. c.-21A>G r.(=) p.(=)