Product Details

SNP ID

rs7744363

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:36456888 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTGGTGTGTTGTCCAGGCTAGTCTC[A/C]TGCAATCCTCCTCTCATGCAAACCT

Phenotype

MIM: 615932

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

KCTD20 PubMed Links

Additional Information

For this assay, SNP(s) [rs4713977] are located under a probe and SNP(s) [rs114588005] 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

Gene

KCTD20

Gene Name

potassium channel tetramerization domain containing 20

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286579.1		Intron			NP_001273508.1
NM_001286580.1		Intron			NP_001273509.1
NM_173562.4		Intron			NP_775833.2
XM_005248940.4		Intron			XP_005248997.1
XM_006715023.2		Intron			XP_006715086.1
XM_011514398.2		Intron			XP_011512700.1

View Full Product Details