Variant #0012461428 (NC_000021.8:g.43645809_43645810insTT, NM_207628.1:c.5_6insTT (ABCG1))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43645809_43645810insTT
DB-ID -
dbSNP ID rs144780823
gnomAD frequency 1/246134
gnomAD homozygote count 0/123024
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.71_72insTT r.(?) p.(Glu25TrpfsTer26)
ABCG1 NM_016818.2 ./. c.71_72insTT r.(?) p.(Glu25TrpfsTer26)
ABCG1 NM_207174.1 ./. c.104_105insTT r.(?) p.(Glu36TrpfsTer26)
ABCG1 NM_207627.1 ./. c.77_78insTT r.(?) p.(Glu27TrpfsTer26)
ABCG1 NM_207628.1 ./. c.5_6insTT r.(?) p.(Glu3TrpfsTer26)
ABCG1 NM_207629.1 ./. c.62_63insTT r.(?) p.(Glu22TrpfsTer26)