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SNP ID

rs61480152

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:122675541 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTCCATTATGTCACTGTTATGAAC[C/T]GCAGATGCTGTGTGTTGCTACTAGC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

OR1L3 PubMed Links

Gene Details

Gene

OR1L3

Gene Name

olfactory receptor family 1 subfamily L member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001005234.1	412	Missense Mutation	CGC,TGC	R138C	NP_001005234.1

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