Product Details

SNP ID
rs12821492
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:116916980 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATCATACAGCAGCTTAGCTTAGCCC[C/T]AAGTGGGCATTCTCAGAGTTACAAG
Phenotype
MIM: 609073
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FBXW8 PubMed Links

Gene Details

Gene
FBXW8
Gene Name
F-box and WD repeat domain containing 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_012174.1 Intron NP_036306.1
NM_153348.2 Intron NP_699179.2
XM_005253867.2 Intron XP_005253924.1
XM_005253868.3 Intron XP_005253925.1
XM_017019175.1 Intron XP_016874664.1
XM_017019176.1 Intron XP_016874665.1
XM_017019177.1 Intron XP_016874666.1
XM_017019178.1 Intron XP_016874667.1

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