Product Details

SNP ID
rs147513716
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.20:44337366 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACATGAATGCCTTACTGGATTATC[A/T]CAACCACATCCGGGCCAGTGTGTAC
Phenotype
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
R3HDML PubMed Links
Additional Information
For this assay, SNP(s) [rs1884612] 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
R3HDML
Gene Name
R3H domain containing like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_178491.3 209 Missense Mutation CAC,CTC H70L NP_848586.1

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