Variant #0001898469 (NC_000002.11:g.169828603A>G, NM_003742.2:c.1435-43delTinsC (ABCB11))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.169828603A>G
DB-ID -
dbSNP ID rs112354931
gnomAD frequency 270/217352
gnomAD homozygote count 3/108409
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.1435-43delTinsC r.(=) p.(=)