Product Details

SNP ID

rs41271312

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:55174618 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGCACCAAATTGGAGGACTCCCCC[A/C]CTTGTCGCAACTGGTCATCTGCTTC

Phenotype

MIM: 602393

Polymorphism

A/C, Transversion 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	346	Missense Mutation	ACT,CCT	T11P	NP_001517.2
XM_017010798.1	346	Missense Mutation	ACT,CCT	T11P	XP_016866287.1

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