Product Details

SNP ID
rs140856583
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:152322985 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCTTTGTGTTTGAGGCTCTGATCC[G/T]CCACACAACTCCCCCACTCCCCCCA
Phenotype
MIM: 606278
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
FBXW7 PubMed Links

Gene Details

Gene
FBXW7
Gene Name
F-box and WD repeat domain containing 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001013415.1 2581 Silent Mutation NP_001013433.1
NM_001257069.1 2581 Intron NP_001243998.1
NM_018315.4 2581 Silent Mutation NP_060785.2
NM_033632.3 2581 Silent Mutation NP_361014.1
XM_011532083.1 2581 Missense Mutation XP_011530385.1
XM_011532084.1 2581 Missense Mutation XP_011530386.1
XM_011532085.1 2581 Missense Mutation XP_011530387.1
XM_011532086.1 2581 Missense Mutation XP_011530388.1
XM_011532087.1 2581 Missense Mutation XP_011530389.1
XM_011532088.1 2581 Missense Mutation XP_011530390.1
XM_017008362.1 2581 Silent Mutation XP_016863851.1

View Full Product Details