Product Details

SNP ID

rs146619785

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:52940004 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAACGCGTCGACTCTGGCGCCGCTG[C/T]CGGCGCCGCTGGCGGTGGCTGTACC

Phenotype

MIM: 600730

Polymorphism

C/T, 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	97	Missense Mutation	CCG,TCG	P33S	NP_005276.2

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