Variant #0001899017 (NC_000002.11:g.169873297_169873305del, NM_003742.2:c.81_89del (ABCB11))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.169873297_169873305del
DB-ID -
dbSNP ID rs777602359
gnomAD frequency 1/227234
gnomAD homozygote count 0/113616
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.81_89del r.(?) p.(Asn27_Asp29del)