Product Details

SNP ID

rs9742

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:37642351 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCCAAACCAACCAGAAGGCTTCCCC[G/T]CTGGGTTGATGGTGGCTTATCATTT

Phenotype

MIM: 606133

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CDC42EP3 PubMed Links

Additional Information

For this assay, SNP(s) [rs115820452] 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

CDC42EP3

Gene Name

CDC42 effector protein 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001270436.1	5246	UTR 3			NP_001257365.1
NM_001270437.1	5246	UTR 3			NP_001257366.1
NM_001270438.1	5246	UTR 3			NP_001257367.1
NM_006449.4	5246	UTR 3			NP_006440.2
XM_011532482.2	5246	UTR 3			XP_011530784.1

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