Variant #0002098853 (NC_000002.11:g.215976357A>T, NM_173076.2:c.126T>A (ABCA12))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.215976357A>T
DB-ID -
dbSNP ID rs779392897
gnomAD frequency 4/245968
gnomAD homozygote count 0/122980
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     
ABCA12 NM_173076.2 ./. c.126T>A r.(?) p.(Ile42=)