Product Details

SNP ID: rs1032592
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.4:143579078 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAGAGTTGACAAAAAAAAAAAAAAG[C/T]GTCTCACTCTACTTGTTACTCTTCT
Phenotype: MIM: 608946
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: FREM3 PubMed Links
Additional Information: For this assay, SNP(s) [rs139763723] 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_001168235.1		Intron			NP_001161707.1