Product Details

SNP ID

rs138784927

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:11658548 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCATTAGGGTGGGACTCTGGGGCTT[C/T]GGGGGTAACCGCTTCATGGGGTGGT

Phenotype

MIM: 605538

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NTSR2 PubMed Links

Additional Information

For this assay, SNP(s) [rs61753869] 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

Gene

NTSR2

Gene Name

neurotensin receptor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012344.3	1238	Silent Mutation	CCA,CCG	P388P	NP_036476.1
XM_005246156.3	1238	UTR 3			XP_005246213.1
XM_006711876.3	1238	UTR 3			XP_006711939.1
XM_006711877.3	1238	UTR 3			XP_006711940.1
XM_017003738.1	1238	UTR 3			XP_016859227.1

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