Product Details
- SNP ID
-
rs10269158
- Assay Type
- Validated
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:87837810 on Build GRCh38
- Set Membership
-
HapMap
Validated
- Context Sequence [VIC/FAM]
- CAATGTCTTGTTTTGAGACCAGCTG[A/G]ATGAAGGGCAAACAATCCTATACTG
- Phenotype
-
MIM: 610821
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
RUNDC3B
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs73706936] 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
- RUNDC3B
- Gene Name
- RUN domain containing 3B
There are no transcripts associated with this gene.
- Gene
- SLC25A40
- Gene Name
- solute carrier family 25 member 40
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_018843.3 |
|
Intron |
|
|
NP_061331.2 |
View Full Product Details