Product Details
- SNP ID
-
rs191156011
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:27129391 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTGGTCTTTCTTCCACTTCATCCTC[C/T]GGTTCTGAAACCAGATCTTGACCTG
- Phenotype
-
MIM: 616068
MIM: 142954
MIM: 142953
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
HOXA-AS2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs2158218] 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
- HOXA-AS2
- Gene Name
- HOXA cluster antisense RNA 2
There are no transcripts associated with this gene.
- Gene
- HOXA3
- Gene Name
- homeobox A3
- Gene
- HOXA4
- Gene Name
- homeobox A4
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_002141.4 |
844 |
Missense Mutation |
CAG,CGG |
Q266R |
NP_002132.3 |
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