Product Details

SNP ID
rs145529777
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:234050812 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGATTTCCAGAATGGAGAAGATGA[C/T]GATGATGATGAAGATATTGATTATG
Phenotype
MIM: 602637
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SPP2 PubMed Links

Gene Details

Gene
SPP2
Gene Name
secreted phosphoprotein 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006944.2 142 Missense Mutation ACG,ATG T9M NP_008875.1
XM_005246102.3 142 Missense Mutation ACG,ATG T9M XP_005246159.1
XM_011511698.2 142 Missense Mutation ACG,ATG T9M XP_011510000.1
XM_011511699.2 142 Missense Mutation ACG,ATG T9M XP_011510001.1
XM_011511700.2 142 Missense Mutation ACG,ATG T9M XP_011510002.1

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