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SNP ID

rs138122203

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:248406229 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAGGAAACCTCAGGTCTTATTTTT[C/G]CCATCATCTCTATCATCTTCTTCAC

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	235	Missense Mutation	CCC,GCC	P79A	NP_112166.1

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