Product Details

SNP ID

rs200094994

Assay Type

Functionally Tested

NCBI dbSNP Submissions

3

Location

Chr.1:31619302 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATGAGTTTCTCCGCTATCTGTGGC[A/G]CGATTATCTGTACCCAAAACAGTAT

Phenotype

MIM: 602392

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

HCRTR1 PubMed Links

Additional Information

For this assay, SNP(s) [rs1056526] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

HCRTR1

Gene Name

hypocretin receptor 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001525.2	986	Missense Mutation	CAC,CGC	H37R	NP_001516.2
XM_017001105.1	986	Missense Mutation	CAC,CGC	H37R	XP_016856594.1
XM_017001106.1	986	Missense Mutation	CAC,CGC	H37R	XP_016856595.1
XM_017001107.1	986	Missense Mutation	CAC,CGC	H37R	XP_016856596.1

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