Variant #0000650206 (NC_000002.11:g.169842746T>C, ABCB11(NM_003742.2):c.957A>G)

Individual ID 00292349
Chromosome 2
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.169842746T>C
DNA change (hg38) g.168986236T>C
Published as -
ISCN -
DB-ID ABCB11_000049 See all 3 reported entries
Variant remarks 145 heterozygous; Clinindb (India)
Reference PubMed: Narang 2020, Journal: Narang 2020
ClinVar ID -
dbSNP ID rs7563233
Origin Germline
Segregation -
Frequency 145/2795 individuals
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.03921 View details
Owner Mohammed Faruq
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCB11 NM_003742.2 -/. - c.957A>G r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000293517 DNA arraySNP - Infinium Global Screening Array v1.0 - 1 Mohammed Faruq