Variant #0000296012 (NC_000012.11:g.21331549T>C, NM_006446.4:c.521T>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.21331549T>C
DNA change (hg38) g.21178615T>C
Published as SLCO1B1(NM_006446.4):c.521T>C (p.V174A), SLCO1B1(NM_006446.5):c.521T>C (p.V174A)
ISCN -
DB-ID SLCO1B1_000001 See all 58 reported entries
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) 0.13262 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

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


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