Product Details

SNP ID

rs115376825

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:231976183 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTGGCTTTTAGTGTACCCATCACC[C/T]CTATAGTGTACATTACAACTCTTTT

Phenotype

MIM: 614184

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

DIS3L2 PubMed Links

Additional Information

For this assay, SNP(s) [rs34169389] 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

DIS3L2

Gene Name

DIS3 like 3'-5' exoribonuclease 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001257281.1		Intron			NP_001244210.1
NM_001257282.1		Intron			NP_001244211.1
NM_152383.4		Intron			NP_689596.4

View Full Product Details