Product Details

SNP ID: hCV29361662
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.11:104888464 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGGTGGTTAGTCATATTATTTTTG[A/T]ATACTAATTGTTTCTTAGATACAAC
Phenotype: MIM: 608633
Polymorphism: A/T, Transversion Substitution
Allele Nomenclature
Literature Links: CASP12 PubMed Links
Additional Information: For this assay, SNP(s) [rs150192515] 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.