Product Details

SNP ID

rs4851126

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:98356161 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGAAGAGTATTTTGGAAAAGTGTTT[C/T]AGAAAAGTTTCAAAGTATGTAGACC

Phenotype

MIM: 600053

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CNGA3 PubMed Links

Additional Information

For this assay, SNP(s) [rs112708953] 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

CNGA3

Gene Name

cyclic nucleotide gated channel alpha 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001079878.1		Intron			NP_001073347.1
NM_001298.2		Intron			NP_001289.1
XM_006712243.2		Intron			XP_006712306.1
XM_011510554.2		Intron			XP_011508856.1

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