Variant #0001899067 (NC_000002.11:g.169874658C>T, NM_003742.2:c.-23G>A (ABCB11))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.169874658C>T
DB-ID -
dbSNP ID rs781079552
gnomAD frequency 6/245546
gnomAD homozygote count 0/122767
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     
ABCB11 NM_003742.2 ./. c.-23G>A r.(=) p.(=)