Product Details

SNP ID
rs73662440
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:120761371 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCACCCAAGAAATCCAATCCTTGT[A/C]AGAAAGGATAGGGCTTATCTTCTCA
Phenotype
MIM: 609071
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
FBXW2 PubMed Links

Gene Details

Gene
FBXW2
Gene Name
F-box and WD repeat domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_012164.3 4599 UTR 3 NP_036296.2
XM_005251910.3 4599 UTR 3 XP_005251967.1
XM_005251913.2 4599 UTR 3 XP_005251970.1
XM_006717049.3 4599 UTR 3 XP_006717112.1
XM_006717051.2 4599 UTR 3 XP_006717114.1
XM_011518518.1 4599 UTR 3 XP_011516820.1
XM_017014615.1 4599 UTR 3 XP_016870104.1
XM_017014616.1 4599 UTR 3 XP_016870105.1
XM_017014617.1 4599 UTR 3 XP_016870106.1

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