Product Details

SNP ID
rs201559666
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:48373562 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTGTTTCCAGGTCACTATCTCTGC[A/C]GAGATGGGACTGCAGCAACTTCACC
Phenotype
MIM: 609075
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
FBXW12 PubMed Links

Gene Details

Gene
FBXW12
Gene Name
F-box and WD repeat domain containing 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001159927.1 155 Missense Mutation CAG,CCG Q48P NP_001153399.1
NM_001159929.1 155 Missense Mutation CAG,CCG Q29P NP_001153401.1
NM_207102.2 155 Missense Mutation CAG,CCG Q48P NP_996985.2
XM_017006224.1 155 Missense Mutation CAG,CCG Q48P XP_016861713.1

View Full Product Details