Product Details
- SNP ID
-
rs143962471
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
16
- Location
-
Chr.1:247672371 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCTCTTGCCTTCTACTGTGCGGATA[C/T]GGAGAATAGCAACAATGATAAAACC
- Phenotype
-
MIM: 611677
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
OR13G1
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs28446289] are located under a probe 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
- OR13G1
- Gene Name
- olfactory receptor family 13 subfamily G member 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001005487.1 |
671 |
Missense Mutation |
CAT,CGT |
H224R |
NP_001005487.1 |
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