Product Details
- SNP ID
-
rs144995082
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:15728525 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCGGTCATGGGGATGGTGGTGACCT[C/T]GGCCATTTTCCAACTGACTTTCTGT
- Phenotype
-
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
OR10H2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs1806931] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- OR10H2
- Gene Name
- olfactory receptor family 10 subfamily H member 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_013939.2 |
502 |
Missense Mutation |
TCG,TTG |
S161L |
NP_039227.1 |
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