Product Details

SNP ID: hCV44533341
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.8:27321497 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAAGTTAAACTAGGTTCAGACTATG[C/T]CCAGGGTAAGCATGGTGGCTGGACG
Phenotype: MIM: 601212
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: PTK2B PubMed Links
Additional Information: For this assay, SNP(s) [rs76595062] 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.