Product Details

SNP ID

rs11867438

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.17:79777483 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

AGAACTCCGGGCAGTTCGTATTACT[A/T]CTTTCTCAGAGTGCTTGGTGGTTTA

Phenotype

MIM: 602770

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

CBX2 PubMed Links

Additional Information

For this assay, SNP(s) [rs74851309] 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

CBX2

Gene Name

chromobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005189.2		Intron			NP_005180.1
NM_032647.3		Intron			NP_116036.1
XM_011525382.1		Intron			XP_011523684.1
XM_011525383.2		Intron			XP_011523685.1

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