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SNP ID: hCV25643514
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:143935401 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GATCAGACTGGACAGCCGACTCCAC[A/G]CTCCCATGTATTTCTTTCTCACCAA
Phenotype: MIM: 608497
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: OR2F1 PubMed Links

Gene Details

Gene: OR2F1
Gene Name: olfactory receptor family 2 subfamily F member 1 (gene/pseudogene)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012369.2	169	Intron			NP_036501.2

Gene: OR2F2
Gene Name: olfactory receptor family 2 subfamily F member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004685.1	169	Missense Mutation	ACT,GCT	T57A	NP_001004685.1

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