Product Details
- SNP ID
-
rs4919378
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:99660958 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- AAATTACACAGCAACTGGGTAGTAA[C/T]GTTTGCCTCTGAGAGATTGTGGGGT
- Phenotype
-
MIM: 616753
MIM: 609767
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
ENTPD7
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs111384276] 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
- ENTPD7
- Gene Name
- ectonucleoside triphosphate diphosphohydrolase 7
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_020354.3 |
|
Intron |
|
|
NP_065087.1 |
- Gene
- SLC25A28
- Gene Name
- solute carrier family 25 member 28
There are no transcripts associated with this gene.
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