Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCCGCCCTCCCACCTTGACGATGC[A/G]GCGATAGGTCTCGTTGTGTGATGCA
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 |
---|---|---|
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 |
AURKB - aurora kinase B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256834.2 | 963 | Missense Mutation | CGC,TGC | R,C 243 | NP_001243763.1 | |
NM_001284526.1 | 963 | Missense Mutation | CGC,TGC | R,C 285 | NP_001271455.1 | |
NM_001313950.1 | 963 | Missense Mutation | CGC,TGC | R,C 284 | NP_001300879.1 | |
NM_001313951.1 | 963 | Intron | NP_001300880.1 | |||
NM_001313952.1 | 963 | Missense Mutation | CGC,TGC | R,C 244 | NP_001300881.1 | |
NM_001313953.1 | 963 | Missense Mutation | CGC,TGC | R,C 252 | NP_001300882.1 | |
NM_001313954.1 | 963 | Missense Mutation | CGC,TGC | R,C 132 | NP_001300883.1 | |
NM_001313955.1 | 963 | Missense Mutation | CGC,TGC | R,C 116 | NP_001300884.1 | |
NM_004217.3 | 963 | Missense Mutation | CGC,TGC | R,C 284 | NP_004208.2 | |
XM_011524070.2 | 963 | Missense Mutation | CGC,TGC | R,C 252 | XP_011522372.1 | |
XM_011524072.2 | 963 | Missense Mutation | CGC,TGC | R,C 243 | XP_011522374.1 | |
XM_017025307.1 | 963 | Missense Mutation | CGC,TGC | R,C 243 | XP_016880796.1 | |
XM_017025308.1 | 963 | Missense Mutation | CGC,TGC | R,C 211 | XP_016880797.1 | |
XM_017025309.1 | 963 | Missense Mutation | CGC,TGC | R,C 132 | XP_016880798.1 | |
XM_017025310.1 | 963 | Missense Mutation | CGC,TGC | R,C 132 | XP_016880799.1 | |
XM_017025311.1 | 963 | Missense Mutation | CGC,TGC | R,C 132 | XP_016880800.1 |