Product Details

SNP ID
rs200008336
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:102236967 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTGGCTGATGGAGGTGGTTTATAC[A/G]AAAAGATTGCAAATCCATTGAAGAA
Phenotype
MIM: 609013
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLCO4C1 PubMed Links

Gene Details

Gene
SLCO4C1
Gene Name
solute carrier organic anion transporter family member 4C1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_180991.4 2031 Missense Mutation TCG,TTG S689L NP_851322.3
XM_011543370.1 2031 Missense Mutation TCG,TTG S601L XP_011541672.1
XM_011543372.1 2031 Missense Mutation TCG,TTG S551L XP_011541674.1

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