Variant #0012461442 (NC_000021.8:g.43645838G>C, NM_207628.1:c.34G>C (ABCG1))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43645838G>C
DB-ID -
dbSNP ID rs753281316
gnomAD frequency 1/246234
gnomAD homozygote count 0/123116
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_004915.3 ./. c.100G>C r.(?) p.(Asp34His)
ABCG1 NM_016818.2 ./. c.100G>C r.(?) p.(Asp34His)
ABCG1 NM_207174.1 ./. c.133G>C r.(?) p.(Asp45His)
ABCG1 NM_207627.1 ./. c.106G>C r.(?) p.(Asp36His)
ABCG1 NM_207628.1 ./. c.34G>C r.(?) p.(Asp12His)
ABCG1 NM_207629.1 ./. c.91G>C r.(?) p.(Asp31His)