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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