Variant #0012461669 (NC_000021.8:g.43702400C>T, NM_207628.1:c.539delCinsT (ABCG1))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43702400C>T
DB-ID -
dbSNP ID -
gnomAD frequency 1/245330
gnomAD homozygote count 0/122663
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.605delCinsT r.(?) p.(Thr202Ile)
ABCG1 NM_016818.2 ./. c.605delCinsT r.(?) p.(Thr202Ile)
ABCG1 NM_207174.1 ./. c.638delCinsT r.(?) p.(Thr213Ile)
ABCG1 NM_207627.1 ./. c.611delCinsT r.(?) p.(Thr204Ile)
ABCG1 NM_207628.1 ./. c.539delCinsT r.(?) p.(Thr180Ile)
ABCG1 NM_207629.1 ./. c.596delCinsT r.(?) p.(Thr199Ile)