Product Details

SNP ID: rs3094478
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.16:2697049 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CACCGGTCTGCCTCTATCCCGCCCC[A/G]ATGCAGCCACTCACGCCCTGGGTGC
Phenotype: MIM: 611285
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: KCTD5 PubMed Links
Additional Information: For this assay, SNP(s) [rs78206812] 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_018992.3		Intron			NP_061865.1