Product Details

SNP ID

rs9907722

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:79780008 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CGGATTGGGCCAGACTTGTTTCTGT[A/G]ATTCTAGATGTCATTTCTATTTTTA

Phenotype

MIM: 602770

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CBX2 PubMed Links

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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