Variant #0012461363 (NC_000021.8:g.43639381T>C, NC_000021.8(NM_207628.1):c.-24-6400T>C (ABCG1))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43639381T>C
DB-ID -
dbSNP ID rs144415936
gnomAD frequency 271/208230
gnomAD homozygote count 3/103847
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.9T>C r.(?) p.(Cys3=)
ABCG1 NM_016818.2 ./. c.9T>C r.(?) p.(Cys3=)
ABCG1 NM_207174.1 ./. c.-701T>C r.(=) p.(=)
ABCG1 NM_207628.1 ./. c.-24-6400T>C r.(=) p.(=)