Product Details

SNP ID
rs28411019
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.14:74321459 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTAAGTGGGGGAACTTGGAAGTAAC[C/T]GGGATGTCTGGCTCCAGAGCCCACA
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
VRTN PubMed Links
Additional Information
For this assay, SNP(s) [rs564056249] 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
VRTN
Gene Name
vertebrae development associated
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018228.2 Intron NP_060698.2
XM_011536911.1 Intron XP_011535213.1

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