Product Details

SNP ID

rs17841732

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.19:532930 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

AGCTGGTCTTGGCCTTTCTCAGAGT[G/C]CACTGAACAGGTGGCTTCTTGGGAC

Phenotype

MIM: 116948

Polymorphism

G/C, Transversion Substitution

Allele Nomenclature

Literature Links

CDC34 PubMed Links

Additional Information

For this assay, SNP(s) [rs17841731] 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

CDC34

Gene Name

cell division cycle 34

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004359.1		Intron			NP_004350.1
XM_005259690.3		Intron			XP_005259747.1
XM_006722952.2		Intron			XP_006723015.1

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