Product Details

SNP ID

rs199644346

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:55174678 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGAAACTCAAGAGCCCTTTTTAAAC[C/T]CCACCGACTATGACGACGAGGAATT

Phenotype

MIM: 602393

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

HCRTR2 PubMed Links

Gene Details

Gene

HCRTR2

Gene Name

hypocretin receptor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001526.3	406	Missense Mutation	CCC,TCC	P31S	NP_001517.2
XM_017010798.1	406	Missense Mutation	CCC,TCC	P31S	XP_016866287.1

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