Product Details

SNP ID

rs145529527

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:142075747 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTTCAGAGATGTCATACGCACCGC[C/T]GAAGAGCTGAGTAGGTAGCTGGTTC

Phenotype

MIM: 162341

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NMBR PubMed Links

Additional Information

For this assay, SNP(s) [rs113235463] 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	751	Silent Mutation	TCA,TCG	S210S	NP_001311236.1
NM_001324308.1	751	Silent Mutation	TCA,TCG	S210S	NP_001311237.1
NM_002511.3	751	Silent Mutation	TCA,TCG	S358S	NP_002502.2
XM_011535846.1	751	Silent Mutation	TCA,TCG	S251S	XP_011534148.1
XM_017010901.1	751	Silent Mutation	TCA,TCG	S269S	XP_016866390.1
XM_017010902.1	751	Silent Mutation	TCA,TCG	S210S	XP_016866391.1

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