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SNP ID: rs186619470
Assay Type: Functionally tested
NCBI dbSNP Submissions: 5
Location: Chr.1:248626440 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACAAGTGGTGAAGGCCTTTTTGCGA[A/C]CTTCAGCAGAGGGCATGCGGTGGAT
Phenotype
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: OR2T10 PubMed Links

Gene Details

Gene: OR2T10
Gene Name: olfactory receptor family 2 subfamily T member 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004693.1	689	Intron			NP_001004693.1
XM_017000273.1	689	Intron			XP_016855762.1

Gene: OR2T11
Gene Name: olfactory receptor family 2 subfamily T member 11 (gene/pseudogene)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001964.1	689	Missense Mutation	GGT,GTT	G230V	NP_001001964.1

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