Product Details

SNP ID

rs140694361

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:7688680 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTTTGGAGACTCAACCGTTAGCTC[C/T]GGACTGCTGTCCTTCAGACCAGGAC

Phenotype

MIM: 191170 MIM: 612661

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

TP53 PubMed Links

Additional Information

For this assay, SNP(s) [rs17880282] 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	187	Missense Mutation	CCG,CTG	P11L	NP_001137462.1
NM_001143991.1	187	Missense Mutation	CCG,CTG	P11L	NP_001137463.1
NM_001143992.1	187	Missense Mutation	CCG,CTG	P11L	NP_001137464.1
NM_018081.2	187	Missense Mutation	CCG,CTG	P11L	NP_060551.2
XM_011523952.2	187	Intron			XP_011522254.1
XM_017024812.1	187	Missense Mutation	CCG,CTG	P11L	XP_016880301.1

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