Variant #0012461445 (NC_000021.8:g.43645853A>G, NM_207628.1:c.49A>G (ABCG1))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43645853A>G
DB-ID -
dbSNP ID rs747843145
gnomAD frequency 1/246242
gnomAD homozygote count 0/123120
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.115A>G r.(?) p.(Ser39Gly)
ABCG1 NM_016818.2 ./. c.115A>G r.(?) p.(Ser39Gly)
ABCG1 NM_207174.1 ./. c.148A>G r.(?) p.(Ser50Gly)
ABCG1 NM_207627.1 ./. c.121A>G r.(?) p.(Ser41Gly)
ABCG1 NM_207628.1 ./. c.49A>G r.(?) p.(Ser17Gly)
ABCG1 NM_207629.1 ./. c.106A>G r.(?) p.(Ser36Gly)