Product Details
- SNP ID
-
rs142118802
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:97994675 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACAATTGCAAATCAAATGATGGAAA[A/C]ATTGAGGGCTTAACAGCTGAATTTG
- Phenotype
-
- Polymorphism
- A/C, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
ANP32B
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs562853890] 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
- ANP32B
- Gene Name
- acidic nuclear phosphoprotein 32 family member B
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_006401.2 |
448 |
Missense Mutation |
AAA,AAC |
K33N |
NP_006392.1 |
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