Product Details

SNP ID

rs36032567

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:26207454 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGGCTCCTCCCTCTTCTCCCAAAA[C/G]TTAAGGCCACTAGCATGATTATAGC

Phenotype

MIM: 604477 MIM: 600124

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

CBX3 PubMed Links

Additional Information

For this assay, SNP(s) [rs78244699] 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

CBX3

Gene Name

chromobox 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007276.4		Intron			NP_009207.2
NM_016587.3		Intron			NP_057671.2
XM_005249611.3		Intron			XP_005249668.1

Gene

HNRNPA2B1

Gene Name

heterogeneous nuclear ribonucleoprotein A2/B1

There are no transcripts associated with this gene.

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