Product Details

SNP ID
rs184362810
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:69673014 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCAGTCTCTTCGTGGAATTCTCCC[C/T]GGGTGCTGAAAGCTGGGCAAGATCT
Phenotype
MIM: 613543
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLCO5A1 PubMed Links

Gene Details

Gene
SLCO5A1
Gene Name
solute carrier organic anion transporter family member 5A1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001146008.1 2944 UTR 3 NP_001139480.1
NM_001146009.1 2944 Missense Mutation NP_001139481.1
NM_030958.2 2944 Missense Mutation NP_112220.2
XM_005251313.2 2944 Missense Mutation XP_005251370.1
XM_017013883.1 2944 UTR 3 XP_016869372.1
XM_017013884.1 2944 Intron XP_016869373.1
XM_017013885.1 2944 Missense Mutation XP_016869374.1
XM_017013886.1 2944 Intron XP_016869375.1

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