Product Details
- SNP ID
-
rs138311368
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:37850663 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTTACCAAGCCTGGTGTGGACCTTG[C/T]AGAGCAATGCAACCTTTATTCAGAA
- Phenotype
-
MIM: 607421
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
NME8
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs2722372] are located under a probe and SNP(s) [rs2598044] 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
- NME8
- Gene Name
- NME/NM23 family member 8
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_016616.4 |
498 |
Silent Mutation |
TGC,TGT |
C42C |
NP_057700.3 |
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