Variant #0002096413 (NC_000002.11:g.215818809G>A, NM_173076.2:c.6416delCinsT (ABCA12))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.215818809G>A
DB-ID -
dbSNP ID rs747323347
gnomAD frequency 2/245560
gnomAD homozygote count 0/122777
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.5462delCinsT r.(?) p.(Thr1821Ile)
ABCA12 NM_173076.2 ./. c.6416delCinsT r.(?) p.(Thr2139Ile)