Product Details
- SNP ID
-
rs144759463
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:110574709 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CACCACCTCCACACACACACAGTGC[C/T]AGAGGTCTCTTGGGTGGACTGGGAC
- Phenotype
-
MIM: 606062
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
SMC3
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs531989525] 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
- SMC3
- Gene Name
- structural maintenance of chromosomes 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_005445.3 |
|
Intron |
|
|
NP_005436.1 |
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