Product Details

SNP ID

rs144638017

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:31619550 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGCAGTCTGCCTGGCCGTGTGGC[A/G]GAACCACCACATGAGGACAGTCACC

Phenotype

MIM: 602392

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

HCRTR1 PubMed Links

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	1094	Missense Mutation	CAG,CGG	Q73R	NP_001516.2
XM_017001105.1	1094	Missense Mutation	CAG,CGG	Q73R	XP_016856594.1
XM_017001106.1	1094	Missense Mutation	CAG,CGG	Q73R	XP_016856595.1
XM_017001107.1	1094	Missense Mutation	CAG,CGG	Q73R	XP_016856596.1

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