Product Details

SNP ID

rs149913884

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:99920991 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCATATTGTTGATTTCCTTCTCAGT[C/T]GCTCTTCTTTGGATTTGAGGCAGAC

Phenotype

MIM: 606111

Polymorphism

C/T, 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	1287	Silent Mutation	GCA,GCG	A324A	NP_001035269.1
NM_032503.2	1287	Silent Mutation	GCA,GCG	A324A	NP_115892.2

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