Product Details

SNP ID
rs202005896
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:92416655 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTATTTTGTAGGTATAGGTGTTCCA[A/G]ATTTCTTGGAATATAGAATGCTTGC
Phenotype
MIM: 611505
Polymorphism
A/G, Transition 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 1273 Intron NP_001012267.1
NM_001286969.1 1273 Intron NP_001273898.1
NM_001286971.1 1273 Intron NP_001273900.1
XM_011518685.2 1273 Intron XP_011516987.1
XM_011518689.1 1273 Intron XP_011516991.1
XM_017014715.1 1273 Intron XP_016870204.1
Gene
OMD
Gene Name
osteomodulin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005014.2 1273 Silent Mutation CTG,TTG L302L NP_005005.1

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