Product Details

SNP ID

rs10739235

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:107285513 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTCAACAGCTCCACTGAAGTATTTA[C/T]GTTCTGTAAGATTTGTTTAGCGTTT

Phenotype

MIM: 600062

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RAD23B PubMed Links

Additional Information

For this assay, SNP(s) [rs114467555] 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

RAD23B

Gene Name

RAD23 homolog B, nucleotide excision repair protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001244713.1		Intron			NP_001231642.1
NM_001244724.1		Intron			NP_001231653.1
NM_002874.4		Intron			NP_002865.1

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