Product Details

SNP ID

rs200337966

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:79834771 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGCCCGCTTCTTGTGGCTGGGGG[A/G]GCGAGCCTCCCCCTCTGCCACCTCG

Phenotype

MIM: 603079

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CBX4 PubMed Links

Additional Information

For this assay, SNP(s) [rs202078528] 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

CBX4

Gene Name

chromobox 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003655.2	2543	Missense Mutation	CCC,TCC	P291S	NP_003646.2
XM_011525399.2	2543	Missense Mutation	CCC,TCC	P225S	XP_011523701.1

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