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SNP ID: rs116716122
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:58031198 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGTACACTTCTGTTACAGTGCCCAA[C/G]ATGCTGGCTGGTTTTATTGGGGTGG
Phenotype
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: OR6Q1 PubMed Links

Gene Details

Gene: OR6Q1
Gene Name: olfactory receptor family 6 subfamily Q member 1 (gene/pseudogene)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001005186.2	246	Missense Mutation	AAC,AAG	N82K	NP_001005186.2

Gene: OR9Q1
Gene Name: olfactory receptor family 9 subfamily Q member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001005212.3	246	Intron			NP_001005212.1

Gene: VN2R9P
Gene Name: vomeronasal 2 receptor 9 pseudogene

There are no transcripts associated with this gene.

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