Product Details
- SNP ID
-
rs146391223
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
17
- Location
-
Chr.1:220881306 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TAGATCCCATTAACGAGGCTTCTGC[A/C]ATCCTGAGTCCCTTAAACTCGAACC
- Phenotype
-
MIM: 142995
- Polymorphism
- A/C, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
HLX
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs140376930] 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
- HLX
- Gene Name
- H2.0 like homeobox
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_021958.3 |
1162 |
Silent Mutation |
GCA,GCC |
A235A |
NP_068777.1 |
- Gene
- HLX-AS1
- Gene Name
- HLX antisense RNA 1
There are no transcripts associated with this gene.
View Full Product Details