Product Details
- SNP ID
-
rs9311
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:196554337 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TTTCTCCATGTTCAATATTTAGCTT[T/C]GGTAAAATGTTGCCATGTTCTTCCT
- Phenotype
-
MIM: 615110
- Polymorphism
- T/C, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
WDR53
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs61730533] 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
- WDR53
- Gene Name
- WD repeat domain 53
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_182627.1 |
1422 |
Silent Mutation |
CCA,CCG |
P317P |
NP_872433.1 |
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