Product Details

SNP ID

rs199763367

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:46834928 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTTCCTAGAGCAACCATTGAGCAG[C/T]CATTATCTGTTGTCTTGGCATCTTG

Phenotype

MIM: 182135

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

HTR2A PubMed Links

Gene Details

Gene

HTR2A

Gene Name

5-hydroxytryptamine receptor 2A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000621.4	1316	Missense Mutation	GAC,GGC	D442G	NP_000612.1
NM_001165947.2	1316	Missense Mutation	GAC,GGC	D358G	NP_001159419.1

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