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SNP ID:
rs9999126
Gene
FBXW7
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.4: 152364655 - 152364655 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

GAATACATAGAGCACATGCTTTTCA[A/G]TATGTGGCTATCATTTGGGCCCTGT

Assay ID C__30087893_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 606278

Literature Links:

 FBXW7 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.07)
(0.93)
Caucasian - Not Available CEPH (CEU)
G (0.02)
(0.98)
EAS
G (0.00)
(1.00)
African American - Not Available YRI (Yoruba)
G (0.21)
(0.79)
SAS
G (0.02)
(0.98)
Chinese - Not Available CHB (Han Chinese)
G (0.01)
(0.99)
AFR
G (0.18)
(0.82)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
G (0.04)
(0.96)
AMR
G (0.04)
(0.96)
FBXW7 - F-box and WD repeat domain containing 7
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid 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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