Product Details

SNP ID

rs11583790

Assay Type

Validated

NCBI dbSNP Submissions

30

Location

Chr.1:22063585 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TAGAGAGGGTCTGTTAGGTGCTTGG[A/G]ATCTTGTTCTTCAACTGCACACATA

Phenotype

MIM: 116952

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CDC42 PubMed Links

Additional Information

For this assay, SNP(s) [rs10158376] 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

CDC42

Gene Name

cell division cycle 42

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039802.1		Intron			NP_001034891.1
NM_001791.3		Intron			NP_001782.1
NM_044472.2		Intron			NP_426359.1

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