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SNP ID

rs140067092

Assay Type

Functionally tested

NCBI dbSNP Submissions

17

Location

Chr.1:158398889 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAATAAAGCCAGCTCTTTCACATGG[G/T]TGTCAGTGCAGGCTAACTTGATAAC

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

OR10T2 PubMed Links

Gene Details

Gene

OR10T2

Gene Name

olfactory receptor family 10 subfamily T member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004475.1	578	Missense Mutation	AAC,ACC	N193T	NP_001004475.1

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