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SNP ID

rs202228770

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:58170289 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGGCTGCTGGATGTCGTCTGGTTC[C/T]TCCTCCTCCTGATGTCCTACTTATT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

OR4D2 PubMed Links

Gene Details

Gene

OR4D2

Gene Name

olfactory receptor family 4 subfamily D member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004707.3	634	Missense Mutation	CTC,TTC	L212F	NP_001004707.1

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