Variant #0012462251 (NC_000021.8:g.43714813C>T, NM_207628.1:c.1706+43delCinsT (ABCG1))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43714813C>T
DB-ID -
dbSNP ID rs543443300
gnomAD frequency 6/244932
gnomAD homozygote count 0/122443
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.1808+43delCinsT r.(=) p.(=)
ABCG1 NM_016818.2 ./. c.1772+43delCinsT r.(=) p.(=)
ABCG1 NM_207174.1 ./. c.1805+43delCinsT r.(=) p.(=)
ABCG1 NM_207627.1 ./. c.1778+43delCinsT r.(=) p.(=)
ABCG1 NM_207628.1 ./. c.1706+43delCinsT r.(=) p.(=)
ABCG1 NM_207629.1 ./. c.1763+43delCinsT r.(=) p.(=)