Product Details

SNP ID

rs9835602

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:12803792 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGAGTTTTCCCAGAAGATGCTGAGA[C/T]AAGGATTCAAATCTAAGTTTATTTG

Phenotype

MIM: 610403

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CAND2 PubMed Links

Additional Information

For this assay, SNP(s) [rs79863133] 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

CAND2

Gene Name

cullin associated and neddylation dissociated 2 (putative)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001162499.1		Intron			NP_001155971.1
NM_012298.2		Intron			NP_036430.1
XM_011533503.2		Intron			XP_011531805.1
XM_011533504.2		Intron			XP_011531806.1

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