Product Details

SNP ID: rs183975963
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.12:21021485 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTTACAGGTATTCTAAAGAAACCAA[C/T]ATTGATCCATCAGAAAATTCAACAT
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: SLCO1B7 PubMed Links

Gene Details

Gene: SLCO1B7
Gene Name: solute carrier organic anion transporter family member 1B7 (putative)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001009562.4	243	Silent Mutation	AAC,AAT	N81N	NP_001009562.3