Product Details

SNP ID

rs11967559

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:142076496 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GATGAAGCAGGGCTTGCTGTTTAAA[A/G]CTACCACTCCACAGGAAAACAAAAT

Phenotype

MIM: 162341

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

NMBR PubMed Links

Additional Information

For this assay, SNP(s) [rs146678853] 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

NMBR

Gene Name

neuromedin B receptor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001324307.1		Intron			NP_001311236.1
NM_001324308.1		Intron			NP_001311237.1
NM_002511.3		Intron			NP_002502.2
XM_011535846.1		Intron			XP_011534148.1
XM_017010901.1		Intron			XP_016866390.1
XM_017010902.1		Intron			XP_016866391.1

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