Product Details

SNP ID
rs143648713
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:102772867 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCACCTCCAGTATTTGTCCGCTGC[A/C]AAGAAGTATGTTTTCTTCTTTTCCT
Phenotype
MIM: 185260
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
MMP10 PubMed Links
Additional Information
For this assay, SNP(s) [rs17860992] 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
MMP10
Gene Name
matrix metallopeptidase 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002425.2 1243 Missense Mutation TTG,TTT L402F NP_002416.1

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