Product Details

SNP ID: rs140559234
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.2:75049523 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCAGTTGGAGGTCAGGTCCAGGGAC[A/G]AGGGTGTGGCCTTGGGGCCGTCCTC
Phenotype: MIM: 162323
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: TACR1 PubMed Links
Additional Information: For this assay, SNP(s) [rs34117315] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001058.3	1718	Missense Mutation	TCG,TTG	S378L	NP_001049.1
NM_015727.2	1718	Intron			NP_056542.1