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SNP ID

rs201770232

Assay Type

Functionally tested

NCBI dbSNP Submissions

5

Location

Chr.1:158398914 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGTCAGTGCAGGCTAACTTGATAA[C/G]AGGTGCCATGTCACAGAAATAGTGG

Phenotype

Polymorphism

C/G, 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	553	Missense Mutation	CTT,GTT	L185V	NP_001004475.1

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