Product Details
- SNP ID
-
rs151291521
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:122937728 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACCCAACACCAAGAATGCGTTCACC[A/G]TGCTTGGTGATGTTTTCCTGACACT
- Phenotype
-
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
C10orf88
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs10794580] 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
- C10orf88
- Gene Name
- chromosome 10 open reading frame 88
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_024942.3 |
1305 |
Silent Mutation |
CAC,CAT |
H360H |
NP_079218.2 |
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