Product Details

SNP ID

rs990192

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:86574165 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCTTGGGGGGGAAAATAACTGCCAG[T/G]CGAAAAGCATAAATTGCAATGGTCT

Phenotype

MIM: 605080

Polymorphism

T/G, Transversion Substitution

Allele Nomenclature

Literature Links

CNGB3 PubMed Links

Additional Information

For this assay, SNP(s) [rs28471019] are located under a probe 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

CNGB3

Gene Name

cyclic nucleotide gated channel beta 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019098.4	4117	UTR 3			NP_061971.3
XM_011517138.2	4117	UTR 3			XP_011515440.1

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