Product Details

SNP ID

rs12169231

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:39132970 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCCGGTGCAGCCGAGAAACCACAT[C/G]TGTATGCCTGGAGCATGGGGTGCCA

Phenotype

MIM: 608457

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

CBX7 PubMed Links

Additional Information

For this assay, SNP(s) [rs138469423] 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

CBX7

Gene Name

chromobox 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_175709.3	1710	UTR 3			NP_783640.1
XM_005261413.4	1710	UTR 3			XP_005261470.1
XM_006724174.3	1710	UTR 3			XP_006724237.1
XM_006724175.3	1710	UTR 3			XP_006724238.1
XM_006724176.3	1710	UTR 3			XP_006724239.1
XM_006724177.3	1710	UTR 3			XP_006724240.1
XM_006724178.3	1710	UTR 3			XP_006724241.1
XM_011530025.2	1710	UTR 3			XP_011528327.1
XM_017028679.1	1710	UTR 3			XP_016884168.1

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