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TCAGCAGAAGGCTTGCTAAAAAAGG[C/T]GTGAGCAGCGGCGTCTGCGAATGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 107271 MIM: 609089 | ||||||||||||||||||||
Literature Links: |
CD59 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 |
CD59 - CD59 molecule | ||||||
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There are no transcripts associated with this gene. |
FBXO3 - F-box protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012175.3 | 1434 | Missense Mutation | NP_036307.2 | |||
NM_033406.2 | 1434 | Intron | NP_208385.1 | |||
XM_011519980.1 | 1434 | Intron | XP_011518282.1 | |||
XM_011519981.2 | 1434 | Intron | XP_011518283.1 | |||
XM_011519982.1 | 1434 | Intron | XP_011518284.1 | |||
XM_017017533.1 | 1434 | Missense Mutation | XP_016873022.1 |