Product Details

SNP ID

rs200367748

Assay Type

Functionally Tested

NCBI dbSNP Submissions

1

Location

Chr.1:182575436 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACCCACTGGCCCCACCAGCTCCAT[C/T]ACACTGAGGCTTGTTTGGACTGTGG

Phenotype

MIM: 180435

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RNASEL PubMed Links

Additional Information

For this assay, SNP(s) [rs36053738] 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

RNASEL

Gene Name

ribonuclease L

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021133.3	2439	Missense Mutation	AAT,GAT	N728D	NP_066956.1

View Full Product Details