Product Details

SNP ID
rs150778647
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:69672988 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGCGCACTGGATCCCTTTTTGCA[A/G]GCCAGTCTCTTCGTGGAATTCTCCC
Phenotype
MIM: 613543
Polymorphism
A/G, 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 2970 UTR 3 NP_001139480.1
NM_001146009.1 2970 Silent Mutation CTG,TTG L755L NP_001139481.1
NM_030958.2 2970 Silent Mutation CTG,TTG L810L NP_112220.2
XM_005251313.2 2970 Silent Mutation CTG,TTG L755L XP_005251370.1
XM_017013883.1 2970 UTR 3 XP_016869372.1
XM_017013884.1 2970 Intron XP_016869373.1
XM_017013885.1 2970 Silent Mutation CTG,TTG L506L XP_016869374.1
XM_017013886.1 2970 Intron XP_016869375.1

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