Variant #0000002435 (NC_000012.12:g.21178691C>T, NM_006446.4:c.597C>T (SLCO1B1))

Individual ID 00000530
Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.21178691C>T
Published as -
Reference Fei Liang Wong et al.(2012)
DB-ID SLCO1B1_000004 See all 4 reported entries
dbSNP ID rs2291075
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-03-21 15:15:00 +08:00 (CST)
Date last edited 2021-08-01 13:28:29 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
SLCO1B1 NM_006446.4 +/. - c.597C>T - r.(=) p.(=) Benign



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000578 DNA MCA;TaqMan SLCO1B1 5 Nur Aisyah Athirah