Product Details

SNP ID

rs146016179

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:152392334 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTCGGTCAGCTCCACAAAGTGGC[A/T]TTCTGTCAGGAAGATGTTCCGCTGG

Phenotype

MIM: 605108

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

NMUR2 PubMed Links

Gene Details

Gene

NMUR2

Gene Name

neuromedin U receptor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020167.4	1271	Missense Mutation	AGC,TGC	S369C	NP_064552.3
XM_011537670.2	1271	Intron			XP_011535972.1

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