Product Details

SNP ID

rs186726581

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:132404757 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGCAGCTGGGGTCCAGCTCCCCCC[C/G]TCCTGCCCGCGGGGTTCAGCCCCCC

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

PWWP2B PubMed Links

Additional Information

For this assay, SNP(s) [rs10747057] are located under a primer 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

PWWP2B

Gene Name

PWWP domain containing 2B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001098637.1	286	Missense Mutation	CCT,CGT	P86R	NP_001092107.1
NM_138499.3	286	Missense Mutation	CCT,CGT	P86R	NP_612508.3
XM_006717659.3	286	Missense Mutation	CCT,CGT	P86R	XP_006717722.1
XM_011539387.2	286	Missense Mutation	CCT,CGT	P86R	XP_011537689.1

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