Product Details

SNP ID: rs114118520
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.13:76884177 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTTTCCTCCCTCCCCACCCCACCCC[A/G]CCCACCAAGTCTTACAGCTAAAGGA
Phenotype: MIM: 610521
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: KCTD12 PubMed Links
Additional Information: For this assay, SNP(s) [rs201622249] 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_138444.3	2229	UTR 3			NP_612453.1