Variant #0012461329 (NC_000021.8:g.43621864G>C, NC_000021.8(NM_207628.1):c.-66+31G>C (ABCG1))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43621864G>C
DB-ID -
dbSNP ID rs769226259
gnomAD frequency 1/243758
gnomAD homozygote count 0/121878
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_207627.1 ./. c.48+31G>C r.(=) p.(=)
ABCG1 NM_207628.1 ./. c.-66+31G>C r.(=) p.(=)