Product Details

SNP ID

rs3804600

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:87231847 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTCAAAGTCTCTATGAAGTACTCC[G/T]TATGTTCCCCTTTTGTGGCATTTCT

Phenotype

MIM: 609512

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CHMP2B PubMed Links

Additional Information

For this assay, SNP(s) [rs77065717] 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

CHMP2B

Gene Name

charged multivesicular body protein 2B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001244644.1		Intron			NP_001231573.1
NM_014043.3		Intron			NP_054762.2
XM_011533576.2		Intron			XP_011531878.1

Gene

MIR4795

Gene Name

microRNA 4795

There are no transcripts associated with this gene.

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