Variant #0000999883 (NC_000012.11:g.21329847G>C, NC_000012.11(NM_006446.4):c.481+16G>C (SLCO1B1))

Chromosome 12
Allele Unknown
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.21329847G>C
DNA change (hg38) -
Published as SLCO1B1(NM_006446.5):c.481+16G>C
ISCN -
DB-ID SLCO1B1_000274
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
SLCO1B1 NM_006446.4 -/. - c.481+16G>C - r.(=) p.(=)


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