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SNP ID

rs142206098

Assay Type

Functionally tested

NCBI dbSNP Submissions

5

Location

Chr.1:248406239 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAGGTCTTATTTTTGCCATCATCT[C/G]TATCATCTTCTTCACCGCACTGATG

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

OR2T1 PubMed Links

Gene Details

Gene

OR2T1

Gene Name

olfactory receptor family 2 subfamily T member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030904.1	245	Missense Mutation	TCT,TGT	S82C	NP_112166.1

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