Product Details

SNP ID: rs17678928
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.17:40149196 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGGCCAGGGTTTTGGTTTGGGTCTC[A/G]GTTTTGCTGTCCAGAGCTCTCATTC
Phenotype: MIM: 606504
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: CASC3 PubMed Links
Additional Information: For this assay, SNP(s) [rs112683299] 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

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007359.4		Intron			NP_031385.2
XM_005257163.1		Intron			XP_005257220.1