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CAGCCACACAGATCTCAATCTGGGC[A/G]CTGTCCAGCAGCTCCTGCCACACCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609094 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FBXO17 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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FBXO17 - F-box protein 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024907.6 | 660 | Silent Mutation | AGC,AGT | S,S 176 | NP_079183.4 | |
NM_148169.2 | 660 | Silent Mutation | AGC,AGT | S,S 185 | NP_680474.1 |