Product Details

SNP ID

rs11960194

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:112985228 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCTAATTACATATGTGTACATGCA[A/G]TATTAGTGTATATTAATATAAATGT

Phenotype

MIM: 609844

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DCP2 PubMed Links

Additional Information

For this assay, SNP(s) [rs79979314] 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

DCP2

Gene Name

decapping mRNA 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001242377.1		Intron			NP_001229306.1
NM_152624.5		Intron			NP_689837.2
XM_017009163.1		Intron			XP_016864652.1

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