Product Details

SNP ID
rs1053446
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:92384479 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGTTTAACTTCAATGTAATGTGTAG[A/T]CTAATACTTTTAGTGGGGTACAAGT
Phenotype
MIM: 611505 MIM: 602383
Polymorphism
A/T, 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 2317 Intron NP_001012267.1
NM_001286969.1 2317 Intron NP_001273898.1
NM_001286971.1 2317 Intron NP_001273900.1
XM_011518685.2 2317 Intron XP_011516987.1
XM_011518689.1 2317 Intron XP_011516991.1
XM_017014715.1 2317 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 2317 UTR 3 NP_054776.1
NM_024416.4 2317 UTR 3 NP_077727.3
NM_033014.3 2317 UTR 3 NP_148935.1

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