Product Details

SNP ID
rs141859598
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:92500873 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAAGGAGACACGGTCCATGCCATC[A/T]TCAGCAAGTTTGTTAAATGACAGGT
Phenotype
MIM: 611505 MIM: 603479
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 1906 Intron NP_001012267.1
NM_001286969.1 1906 Intron NP_001273898.1
NM_001286971.1 1906 Intron NP_001273900.1
XM_011518685.2 1906 Intron XP_011516987.1
XM_011518689.1 1906 Intron XP_011516991.1
XM_017014715.1 1906 Intron XP_016870204.1
Gene
ECM2
Gene Name
extracellular matrix protein 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001197295.1 1906 Missense Mutation GAA,GAT E573D NP_001184224.1
NM_001197296.1 1906 Missense Mutation GAA,GAT E573D NP_001184225.1
NM_001393.3 1906 Missense Mutation GAA,GAT E595D NP_001384.1
XM_017014376.1 1906 Intron XP_016869865.1
XM_017014377.1 1906 Intron XP_016869866.1

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