Product Details

SNP ID
rs665653
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:95173316 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGAAGTTCAGCTTGCATTCGTGCT[C/T]CCATTAAAAGTAGATTGACATGAAC
Phenotype
MIM: 607768
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SESN3 PubMed Links

Gene Details

Gene
SESN3
Gene Name
sestrin 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001271594.1 1744 Missense Mutation GAA,GGA E334G NP_001258523.1
NM_144665.3 1744 Missense Mutation GAA,GGA E473G NP_653266.2
XM_011542614.1 1744 Missense Mutation GAA,GGA E450G XP_011540916.1

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