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TCTAGAATCAAGTAGATCCTCCTCC[A/G]GTCATAAAAATAGTTGTAGAGACGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604970 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
AURKB 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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AURKB - aurora kinase B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256834.2 | 552 | Missense Mutation | CGG,TGG | R,W 106 | NP_001243763.1 | |
NM_001284526.1 | 552 | Missense Mutation | CGG,TGG | R,W 148 | NP_001271455.1 | |
NM_001313950.1 | 552 | Missense Mutation | CGG,TGG | R,W 147 | NP_001300879.1 | |
NM_001313951.1 | 552 | Intron | NP_001300880.1 | |||
NM_001313952.1 | 552 | Missense Mutation | CGG,TGG | R,W 107 | NP_001300881.1 | |
NM_001313953.1 | 552 | Missense Mutation | CGG,TGG | R,W 115 | NP_001300882.1 | |
NM_001313954.1 | 552 | UTR 5 | NP_001300883.1 | |||
NM_001313955.1 | 552 | Intron | NP_001300884.1 | |||
NM_004217.3 | 552 | Missense Mutation | CGG,TGG | R,W 147 | NP_004208.2 | |
XM_011524070.2 | 552 | Missense Mutation | CGG,TGG | R,W 115 | XP_011522372.1 | |
XM_011524072.2 | 552 | Missense Mutation | CGG,TGG | R,W 106 | XP_011522374.1 | |
XM_017025307.1 | 552 | Missense Mutation | CGG,TGG | R,W 106 | XP_016880796.1 | |
XM_017025308.1 | 552 | Missense Mutation | CGG,TGG | R,W 74 | XP_016880797.1 | |
XM_017025309.1 | 552 | UTR 5 | XP_016880798.1 | |||
XM_017025310.1 | 552 | UTR 5 | XP_016880799.1 | |||
XM_017025311.1 | 552 | UTR 5 | XP_016880800.1 |