Product Details

SNP ID
rs201678753
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:11658540 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCTCTGCCTGCCCCCAGCACCTGC[C/T]TCAAGTCCCAGGTGGTGGACCTCAA
Phenotype
MIM: 607112 MIM: 609111 MIM: 605647
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FBXO2 PubMed Links

Gene Details

Gene
FBXO2
Gene Name
F-box protein 2
There are no transcripts associated with this gene.

Gene
FBXO44
Gene Name
F-box protein 44
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001014765.1 499 Missense Mutation CTC,TTC L134F NP_001014765.1
NM_001304790.1 499 Intron NP_001291719.1
NM_001304791.1 499 Missense Mutation CTC,TTC L134F NP_001291720.1
NM_033182.5 499 Missense Mutation CTC,TTC L134F NP_149438.2
NM_183412.2 499 Intron NP_904319.1
NM_183413.2 499 Intron NP_904320.1
XM_005263535.1 499 Missense Mutation CCT,CTT P124L XP_005263592.1
XM_005263536.4 499 Missense Mutation CCT,CTT P124L XP_005263593.1
XM_005263537.1 499 Missense Mutation CCT,CTT P124L XP_005263594.1
XM_006711043.2 499 Missense Mutation CCT,CTT P124L XP_006711106.1
XM_006711045.2 499 Missense Mutation CTC,TTC L134F XP_006711108.1
XM_011542435.1 499 Missense Mutation CCT,CTT P124L XP_011540737.1
XM_017002842.1 499 Missense Mutation CCT,CTT P124L XP_016858331.1
XM_017002843.1 499 Missense Mutation CTC,TTC L134F XP_016858332.1
XM_017002844.1 499 Intron XP_016858333.1
Gene
FBXO6
Gene Name
F-box protein 6
There are no transcripts associated with this gene.

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