Product Details

SNP ID
rs201186715
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.13:40559803 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGCATGGGGTGGGGCAGAGGCACT[G/T]GTACAGGTGTCTTCACTTGGGTCAG
Phenotype
MIM: 136533
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
FOXO1 PubMed Links

Gene Details

Gene
FOXO1
Gene Name
forkhead box O1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002015.3 2073 Missense Mutation CAA,CCA Q563P NP_002006.2
XM_011535008.2 2073 Missense Mutation CAA,CCA Q382P XP_011533310.1
XM_011535010.2 2073 Missense Mutation CAA,CCA Q326P XP_011533312.1

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