Product Details

SNP ID
rs139398811
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.13:40559830 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TACAGGTGTCTTCACTTGGGTCAGG[C/T]GGTTCATACCCGAGGTGTGGGGCAT
Phenotype
MIM: 136533
Polymorphism
C/T, Transition 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 2046 Missense Mutation CCC,CTC P554L NP_002006.2
XM_011535008.2 2046 Missense Mutation CCC,CTC P373L XP_011533310.1
XM_011535010.2 2046 Missense Mutation CCC,CTC P317L XP_011533312.1

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