Product Details

SNP ID

rs2236529

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:92385802 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCTATGTTGTTGAACTGAAAAAAAA[A/C]GAGGAAAACATTGTTCAGAAATCTG

Phenotype

MIM: 611505 MIM: 602383

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

CENPP PubMed Links

Gene Details

Gene

CENPP

Gene Name

centromere protein P

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012267.2		Intron			NP_001012267.1
NM_001286969.1		Intron			NP_001273898.1
NM_001286971.1		Intron			NP_001273900.1
XM_011518685.2		Intron			XP_011516987.1
XM_011518689.1		Intron			XP_011516991.1
XM_017014715.1		Intron			XP_016870204.1

Gene

OGN

Gene Name

osteoglycin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014057.4		Intron			NP_054776.1
NM_024416.4		Intron			NP_077727.3
NM_033014.3		Intron			NP_148935.1

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