Product Details

SNP ID

rs115328679

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:231109129 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACCATCCAGCATTGCCACCTTTTC[C/T]GGTGACGAGCAAGGTGTTTCATCCC

Phenotype

MIM: 601122

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

HTR2B PubMed Links

Gene Details

Gene

HTR2B

Gene Name

5-hydroxytryptamine receptor 2B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000867.4	1289	Silent Mutation	CCA,CCG	P278P	NP_000858.3
NM_001320758.1	1289	Silent Mutation	CCA,CCG	P236P	NP_001307687.1
XM_005246520.3	1289	Silent Mutation	CCA,CCG	P159P	XP_005246577.1
XM_006712482.2	1289	Silent Mutation	CCA,CCG	P253P	XP_006712545.1

Gene

PSMD1

Gene Name

proteasome 26S subunit, non-ATPase 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001191037.1	1289	Intron			NP_001177966.1
NM_002807.3	1289	Intron			NP_002798.2
XM_017004517.1	1289	Intron			XP_016860006.1

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