Variant #0012461316 (NC_000021.8:g.43621810A>G, NM_207628.1:c.-89A>G (ABCG1))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43621810A>G
DB-ID -
dbSNP ID -
gnomAD frequency 1/243348
gnomAD homozygote count 0/121673
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     
ABCG1 NM_207627.1 ./. c.25A>G r.(?) p.(Lys9Glu)
ABCG1 NM_207628.1 ./. c.-89A>G r.(=) p.(=)