Product Details

SNP ID
rs4315757
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:152326991 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATCCCTTAAACATTTGGTTCAACAT[C/T]AGCGCTATACTCTTCTGAAAACCAG
Phenotype
MIM: 606278
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FBXW7 PubMed Links

Gene Details

Gene
FBXW7
Gene Name
F-box and WD repeat domain containing 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001013415.1 Intron NP_001013433.1
NM_001257069.1 Intron NP_001243998.1
NM_018315.4 Intron NP_060785.2
NM_033632.3 Intron NP_361014.1
XM_011532083.1 Intron XP_011530385.1
XM_011532084.1 Intron XP_011530386.1
XM_011532085.1 Intron XP_011530387.1
XM_011532086.1 Intron XP_011530388.1
XM_011532087.1 Intron XP_011530389.1
XM_011532088.1 Intron XP_011530390.1
XM_017008362.1 Intron XP_016863851.1

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