Product Details

SNP ID
rs200460052
Assay Type
Functionally Tested
NCBI dbSNP Submissions
8
Location
Chr.1:232805421 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCTTCAGCTTCTCGTTTGCGGAGC[C/G]CGCGGCGGCGTTTCCTGGGGCAACA
Phenotype
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
MAP10 PubMed Links
Additional Information
For this assay, SNP(s) [rs12409898] 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
MAP10
Gene Name
microtubule associated protein 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_019090.2 530 Missense Mutation CCC,CGC P133R NP_061963.2

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