Variant #0002096985 (NC_000002.11:g.215843169C>T, NM_173076.2:c.4999delGinsA (ABCA12))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.215843169C>T
DB-ID -
dbSNP ID rs769950193
gnomAD frequency 1/244824
gnomAD homozygote count 0/122410
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.4045delGinsA r.(?) p.(Glu1349Lys)
ABCA12 NM_173076.2 ./. c.4999delGinsA r.(?) p.(Glu1667Lys)