Product Details

SNP ID

rs61735377

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:152392313 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATGGGAATTGGGGACCTATATCTT[C/T]GGTCAGCTCCACAAAGTGGCATTCT

Phenotype

MIM: 605108

Polymorphism

C/T, Transition 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	1292	Missense Mutation	AAA,GAA	K376E	NP_064552.3
XM_011537670.2	1292	Intron			XP_011535972.1

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