Product Details

SNP ID

rs148082432

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:52940272 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTATCGACCAGTACAACACCTTCT[C/G]CAGCCTCTACTTCCTCACCGTCATG

Phenotype

MIM: 600730

Polymorphism

C/G, Transversion 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	365	Missense Mutation	TCC,TGC	S122C	NP_005276.2

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