Product Details

SNP ID
rs140414155
Assay Type
Functionally tested
NCBI dbSNP Submissions
11
Location
Chr.1:16250908 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTACATCTGCATGGGCTTGCAGTTC[A/G]TACTCTGGTATAGGGGTTTGCCAAC
Phenotype
MIM: 609109
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FBXO42 PubMed Links

Gene Details

Gene
FBXO42
Gene Name
F-box protein 42
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018994.2 2170 Missense Mutation ACG,ATG T639M NP_061867.1
XM_006710698.3 2170 Missense Mutation ACG,ATG T639M XP_006710761.1
XM_017001502.1 2170 Missense Mutation ACG,ATG T408M XP_016856991.1
XM_017001503.1 2170 Missense Mutation ACG,ATG T408M XP_016856992.1

View Full Product Details