Product Details

SNP ID

rs201692578

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:99921095 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGCATAGCTGAGACAGATGGAGA[A/G]GTAATAACCCACATAGAAGGCCAGT

Phenotype

MIM: 606111

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MCHR2 PubMed Links

Gene Details

Gene

MCHR2

Gene Name

melanin concentrating hormone receptor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040179.1	1183	Missense Mutation	CTC,TTC	L290F	NP_001035269.1
NM_032503.2	1183	Missense Mutation	CTC,TTC	L290F	NP_115892.2

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