Product Details
- SNP ID
-
rs112212538
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:35906604 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CACCACCTCCACCACCACCACCACC[A/C]CCACCGCCACCATCCCCGCCACGCT
- Phenotype
-
- Polymorphism
- A/C, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
HRCT1
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs79284865] 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
- HRCT1
- Gene Name
- histidine rich carboxyl terminus 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001039792.1 |
413 |
Missense Mutation |
CAC,CCC |
H106P |
NP_001034881.1 |
- Gene
- LINC00961
- Gene Name
- long intergenic non-protein coding RNA 961
There are no transcripts associated with this gene.
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