Product Details

SNP ID
rs200313002
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:7688852 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTCAGCTGTGTCCCAGGAGCTACG[C/G]GAGGGGGACCCAGTTTCTCTCTCCA
Phenotype
MIM: 191170 MIM: 612661
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
TP53 PubMed Links
Additional Information
For this assay, SNP(s) [rs2287499] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
TP53
Gene Name
tumor protein p53
There are no transcripts associated with this gene.

Gene
WRAP53
Gene Name
WD repeat containing antisense to TP53
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001143990.1 359 Silent Mutation CGC,CGG R68R NP_001137462.1
NM_001143991.1 359 Silent Mutation CGC,CGG R68R NP_001137463.1
NM_001143992.1 359 Silent Mutation CGC,CGG R68R NP_001137464.1
NM_018081.2 359 Silent Mutation CGC,CGG R68R NP_060551.2
XM_011523952.2 359 UTR 5 XP_011522254.1
XM_017024812.1 359 Silent Mutation CGC,CGG R68R XP_016880301.1

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