Product Details

SNP ID: rs1333124
Assay Type: Validated
NCBI dbSNP Submissions: 63
Location: Chr.1:108715528 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: GGTGTAAAACAGACAATCTCTCTCT[C/T]CAGCCTGTGTTTGCCGCATACTCCT
Phenotype
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: FNDC7 PubMed Links
Additional Information: For this assay, SNP(s) [rs116828353] 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_001144937.1		Intron			NP_001138409.1