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TAAGGACCTTTCAGAGAGACCTTTT[C/T]TGACAAATGAGGTAGAAATCACACT
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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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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 | 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 |