Product Details

SNP ID
rs34315986
Assay Type
Functionally Tested
NCBI dbSNP Submissions
21
Location
Chr.1:28259865 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGCGCACCATGATCGTGGCGGACTC[C/G]GAGTGCCGCGCAGAGCTCAAGGACT
Phenotype
MIM: 607767
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
SESN2 PubMed Links

Gene Details

Gene
SESN2
Gene Name
sestrin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_031459.4 414 Silent Mutation TCC,TCG S6S NP_113647.1

View Full Product Details