Product Details

SNP ID
rs199636063
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:32475369 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCCGGCTCCTGGAGAACATGGCCC[A/G]GCCTCCCGGGGGCTCTGGTCCCCTC
Phenotype
MIM: 605648
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FBXO7 PubMed Links

Gene Details

Gene
FBXO7
Gene Name
F-box protein 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001033024.1 133 Missense Mutation CAG,CGG Q3R NP_001028196.1
NM_001257990.1 133 UTR 5 NP_001244919.1
NM_012179.3 133 Intron NP_036311.3
XM_011530106.1 133 Intron XP_011528408.1

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