Variant #0012461338 (NC_000021.8:g.43636250C>A, NC_000021.8(NM_207628.1):c.-25+9154C>A (ABCG1))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43636250C>A
DB-ID -
dbSNP ID rs764826860
gnomAD frequency 8/121338
gnomAD homozygote count 0/60653
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.-3123C>A r.(=) p.(=)
ABCG1 NM_016818.2 ./. c.-3123C>A r.(=) p.(=)
ABCG1 NM_207174.1 ./. c.-3832C>A r.(=) p.(=)
ABCG1 NM_207628.1 ./. c.-25+9154C>A r.(=) p.(=)
ABCG1 NM_207629.1 ./. c.-16C>A r.(=) p.(=)