Product Details
- SNP ID
-
rs10022491
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:40335891 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TTAATGACCTTTTTGAAGATTATTC[C/T]AATGCTCTTCGTCCAGTGGAAGATA
- Phenotype
-
MIM: 605116
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
CHRNA9
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs55974552] 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
- CHRNA9
- Gene Name
- cholinergic receptor nicotinic alpha 9 subunit
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_017581.3 |
268 |
Silent Mutation |
TCC,TCT |
S43S |
NP_060051.2 |
- Gene
- LOC101060498
- Gene Name
- uncharacterized LOC101060498
There are no transcripts associated with this gene.
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