Product Details
- SNP ID
-
rs9420589
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:92690476 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAAAAGCGATGGAAAAGCAGCTGTC[G/T]GGCACGCGCGGGGACGGGAGGCGCG
- Phenotype
-
MIM: 604420
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
HHEX
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs117662920] 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
- HHEX
- Gene Name
- hematopoietically expressed homeobox
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_002729.4 |
|
Intron |
|
|
NP_002720.1 |
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