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SNP ID

rs149101016

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:55665362 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTATTTTTTTCTTACCTTCTTGTCC[C/T]TTTTGGATGTCATGTTCTCATCTGT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

OR4C6 PubMed Links

Gene Details

Gene

OR4C6

Gene Name

olfactory receptor family 4 subfamily C member 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004704.1	196	Missense Mutation	CTT,TTT	L66F	NP_001004704.1

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