Variant #0000002605 (NC_000012.12:g.21178615T>C, NM_006446.4:c.521T>C (SLCO1B1))

Individual ID 00000581
Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.21178615T>C
Published as -
Reference Feiliang Wong et al.(2013)
DB-ID SLCO1B1_000002 See all 5 reported entries
dbSNP ID rs4149056
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 2021-04-12 11:44:29 +08:00 (CST)
Date last edited 2021-08-01 14:09:40 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

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DNA change (cDNA)     

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Protein     

Clinical classification     
SLCO1B1 NM_006446.4 +/. - c.521T>C - r.(?) p.(Val174Ala) -



Screenings


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Genes screened     

Variants found     

Owner     
0000000642 DNA MCA SLCO1B1 2 Nur Aisyah Athirah