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TTTTCTAATTTTCTTTCTTAACTCA[A/T]ATATTAGCTAGCAATAGATCTTTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609083 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FBXL17 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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FBXL17 - F-box and leucine rich repeat protein 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001163315.2 | 3632 | UTR 3 | NP_001156787.2 | |||
XM_005272048.4 | 3632 | Intron | XP_005272105.1 | |||
XM_005272050.4 | 3632 | Intron | XP_005272107.1 | |||
XM_011543574.2 | 3632 | Intron | XP_011541876.1 | |||
XM_011543575.2 | 3632 | Intron | XP_011541877.1 | |||
XM_011543576.2 | 3632 | Intron | XP_011541878.1 | |||
XM_011543577.2 | 3632 | Intron | XP_011541879.1 | |||
XM_011543578.2 | 3632 | Intron | XP_011541880.1 | |||
XM_011543579.2 | 3632 | Intron | XP_011541881.1 | |||
XM_011543580.2 | 3632 | Intron | XP_011541882.1 | |||
XM_017009729.1 | 3632 | Intron | XP_016865218.1 |