Variant #0002098444 (NC_000002.11:g.215896604T>C, NM_173076.2:c.1002A>G (ABCA12))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.215896604T>C
DB-ID -
dbSNP ID -
gnomAD frequency 1/246112
gnomAD homozygote count 0/123055
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_015657.3 ./. c.48A>G r.(?) p.(Ile16Met)
ABCA12 NM_173076.2 ./. c.1002A>G r.(?) p.(Ile334Met)