Product Details

SNP ID

rs142523561

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:92385680 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAATAAAACTGTTTGGATGCTTTCC[C/G]AGGACGATTGGATTGCCCTCCAGGC

Phenotype

MIM: 611505 MIM: 602383

Polymorphism

C/G, 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	1116	Intron			NP_001012267.1
NM_001286969.1	1116	Intron			NP_001273898.1
NM_001286971.1	1116	Intron			NP_001273900.1
XM_011518685.2	1116	Intron			XP_011516987.1
XM_011518689.1	1116	Intron			XP_011516991.1
XM_017014715.1	1116	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	1116	Silent Mutation	CTC,CTG	L279L	NP_054776.1
NM_024416.4	1116	Silent Mutation	CTC,CTG	L337L	NP_077727.3
NM_033014.3	1116	Silent Mutation	CTC,CTG	L279L	NP_148935.1

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