Product Details

SNP ID: rs140492814
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.11:114439660 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGGAGAGCATGGCTCAGCGGATGGT[C/T]TGGGTGGACCTGGAGGTGAGTGAGG
Phenotype: MIM: 607149
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: REXO2 PubMed Links
Additional Information: For this assay, SNP(s) [rs476200] 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_015523.3	275	Silent Mutation	GTC,GTT	V44V	NP_056338.2