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SNP ID

rs149625259

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:3356185 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTACTAGTTCAGTCCCCCAAATGC[C/T]GATCAATTTATGGGGACCAGGCAAG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

OR2C1 PubMed Links

Gene Details

Gene

OR2C1

Gene Name

olfactory receptor family 2 subfamily C member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012368.2	297	Missense Mutation	CCG,CTG	P82L	NP_036500.2

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