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Search Thermo Fisher Scientific
AATTCCCTGTCTCCACATCCCAAAC[A/G]CGGATTGATGTATCAAGAGATCCAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606278 | ||||||||||||||||||||
Literature Links: |
FBXW7 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
FBXW7 - F-box and WD repeat domain containing 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001013415.1 | 2253 | Silent Mutation | CGC,CGT | R,R 446 | NP_001013433.1 | |
NM_001257069.1 | 2253 | Intron | NP_001243998.1 | |||
NM_018315.4 | 2253 | Silent Mutation | CGC,CGT | R,R 484 | NP_060785.2 | |
NM_033632.3 | 2253 | Silent Mutation | CGC,CGT | R,R 564 | NP_361014.1 | |
XM_011532083.1 | 2253 | Silent Mutation | CGC,CGT | R,R 564 | XP_011530385.1 | |
XM_011532084.1 | 2253 | Silent Mutation | CGC,CGT | R,R 564 | XP_011530386.1 | |
XM_011532085.1 | 2253 | Silent Mutation | CGC,CGT | R,R 564 | XP_011530387.1 | |
XM_011532086.1 | 2253 | Silent Mutation | CGC,CGT | R,R 536 | XP_011530388.1 | |
XM_011532087.1 | 2253 | Silent Mutation | CGC,CGT | R,R 536 | XP_011530389.1 | |
XM_011532088.1 | 2253 | Silent Mutation | CGC,CGT | R,R 397 | XP_011530390.1 | |
XM_017008362.1 | 2253 | Silent Mutation | CGC,CGT | R,R 564 | XP_016863851.1 |