Product Details
- SNP ID
-
rs202210130
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.12:53938967 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGAGAGCCTTATGTACGTCTATGAG[A/G]ACAGCGCGGCGGAGAGCGGCATCGG
- Phenotype
-
MIM: 142976
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
HOXC13
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs535209331] 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
- HOXC13
- Gene Name
- homeobox C13
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_017410.2 |
176 |
Missense Mutation |
AAC,GAC |
N21D |
NP_059106.2 |
- Gene
- HOXC13-AS
- Gene Name
- HOXC13 antisense RNA
There are no transcripts associated with this gene.
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