Product Details

SNP ID

rs202246026

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:55174745 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGGAATACCTGCACCCGAAAGAAT[A/G]TGAGTGGGTCCTGATCGCCGGGTAC

Phenotype

MIM: 602393

Polymorphism

A/G, 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	473	Missense Mutation	TAT,TGT	Y53C	NP_001517.2
XM_017010798.1	473	Missense Mutation	TAT,TGT	Y53C	XP_016866287.1

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