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SNP ID

rs141900029

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:20223833 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGTTTCCATGGTCAAAGGGAGATG[A/C]AGAGCTGCTTCTTCTCATTCATCCT

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

OR11H6 PubMed Links

Gene Details

Gene

OR11H6

Gene Name

olfactory receptor family 11 subfamily H member 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004480.1	124	Missense Mutation	AAG,CAG	K42Q	NP_001004480.1

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