Product Details

SNP ID

rs147171381

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:52940436 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGTCGTGCTGCCCTTCGCAGTCTTC[A/G]CCCGGCTAGACGACGAGCAGGGCCG

Phenotype

MIM: 600730

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

NPBWR1 PubMed Links

Gene Details

Gene

NPBWR1

Gene Name

neuropeptides B/W receptor 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005285.3	529	Missense Mutation	ACC,GCC	T177A	NP_005276.2

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