Product Details

SNP ID: rs519176
Assay Type: Functionally tested
NCBI dbSNP Submissions: 56
Location: Chr.1:28260473 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGGCCAGTGAAAGTCGACCTCATCC[C/T]ATGTCCACCGCACTCCTGCTTTGGA
Phenotype: MIM: 607767
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: SESN2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031459.4		Intron			NP_113647.1