Product Details

SNP ID: rs1876803
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.3:185080279 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AATACATAAGGTGATTATCAACTAT[C/T]ATTAAATCCAAAAATTCCATTAAAA
Phenotype
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: C3orf70 PubMed Links
Additional Information: For this assay, SNP(s) [rs113805911] 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

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001025266.1	3672	UTR 3			NP_001020437.1