Product Details

SNP ID

rs143501297

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:178149741 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGGGGTAGGGGCAGGGACTGCACC[G/T]CCTCCAGGCACTCATCGTAAGCCTC

Phenotype

MIM: 606470

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

NHP2 PubMed Links

Additional Information

For this assay, SNP(s) [rs147575606] 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

NHP2

Gene Name

NHP2 ribonucleoprotein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001034833.1		Intron			NP_001030005.1
NM_017838.3		Intron			NP_060308.1

Gene

RMND5B

Gene Name

required for meiotic nuclear division 5 homolog B

There are no transcripts associated with this gene.

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