Variant #0000972054 (NC_000002.11:g.169842641A>T, NM_003742.2:c.1062T>A (ABCB11))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.169842641A>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID ABCB11_000087
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs376258647
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-03-27 14:47:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCB11 NM_003742.2 +/. - c.1062T>A r.(?) p.(Tyr354Ter)


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