Variant #0012461436 (NC_000021.8:g.43645822G>A, NM_207628.1:c.18G>A (ABCG1))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43645822G>A
DB-ID -
dbSNP ID rs751989691
gnomAD frequency 6/246204
gnomAD homozygote count 0/123095
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     
ABCG1 NM_004915.3 ./. c.84G>A r.(?) p.(Ser28=)
ABCG1 NM_016818.2 ./. c.84G>A r.(?) p.(Ser28=)
ABCG1 NM_207174.1 ./. c.117G>A r.(?) p.(Ser39=)
ABCG1 NM_207627.1 ./. c.90G>A r.(?) p.(Ser30=)
ABCG1 NM_207628.1 ./. c.18G>A r.(?) p.(Ser6=)
ABCG1 NM_207629.1 ./. c.75G>A r.(?) p.(Ser25=)