Product Details

SNP ID: hCV30947112
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.15:101639969 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGGCATTACTGGGGTAAATGGAAGA[G/T]AGCTGACAAAGCAAGGTAGAGATTC
Phenotype: MIM: 610014
Polymorphism: G/T, Transversion Substitution
Allele Nomenclature
Literature Links: TM2D3 PubMed Links
Additional Information: For this assay, SNP(s) [rs141759201] 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

There are no transcripts associated with this gene.