Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGCCCTCCCTCTCCCTGCAGGTTC[A/G]CAGCCAGGCCAGATTGCGGGTCCAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
19 submissions
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Phenotype: |
MIM: 607112 MIM: 609111 MIM: 605647 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FBXO2 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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FBXO2 - F-box protein 2 | ||||||
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There are no transcripts associated with this gene. |
FBXO44 - F-box protein 44 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001014765.1 | 592 | Missense Mutation | ACA,GCA | T,A 165 | NP_001014765.1 | |
NM_001304790.1 | 592 | Missense Mutation | CAC,CGC | H,R 123 | NP_001291719.1 | |
NM_001304791.1 | 592 | Missense Mutation | ACA,GCA | T,A 165 | NP_001291720.1 | |
NM_033182.5 | 592 | Missense Mutation | ACA,GCA | T,A 165 | NP_149438.2 | |
NM_183412.2 | 592 | Missense Mutation | CAC,CGC | H,R 123 | NP_904319.1 | |
NM_183413.2 | 592 | Missense Mutation | CAC,CGC | H,R 123 | NP_904320.1 | |
XM_005263535.1 | 592 | Missense Mutation | CAC,CGC | H,R 155 | XP_005263592.1 | |
XM_005263536.4 | 592 | Missense Mutation | CAC,CGC | H,R 155 | XP_005263593.1 | |
XM_005263537.1 | 592 | Missense Mutation | CAC,CGC | H,R 155 | XP_005263594.1 | |
XM_006711043.2 | 592 | Missense Mutation | CAC,CGC | H,R 155 | XP_006711106.1 | |
XM_006711045.2 | 592 | Missense Mutation | ACA,GCA | T,A 165 | XP_006711108.1 | |
XM_011542435.1 | 592 | Missense Mutation | CAC,CGC | H,R 155 | XP_011540737.1 | |
XM_017002842.1 | 592 | Missense Mutation | CAC,CGC | H,R 155 | XP_016858331.1 | |
XM_017002843.1 | 592 | Missense Mutation | ACA,GCA | T,A 165 | XP_016858332.1 | |
XM_017002844.1 | 592 | Missense Mutation | CAC,CGC | H,R 123 | XP_016858333.1 |
FBXO6 - F-box protein 6 | ||||||
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There are no transcripts associated with this gene. |