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Summary

Isoform:
Position:
284
Ref:
T
Mutation:
I
PTM impact:
direct
PTM affected:
3
Kinases:
AURKB

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

Li-Fraumeni syndrome, Hereditary cancer-predisposing syndrome

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 284T

Affected site:

Position: 284
Residue: T
Type: phosphorylation

Impact:

direct

Other known mutations affecting this site

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Mutation
In sequence
Distance
Impact
284I CPGRDRR[T/I]TEEENLRK 0
direct
284S CPGRDRR[T/S]TEEENLRK 0
direct
284A CPGRDRR[T/A]TEEENLRK 0
direct
284P CPGRDRR[T/P]TEEENLRK 0
direct
285V CPGRDRRT[E/V]EEENLRK 1
proximal
Showing 1 to 5 of 51 rows

PTM Site: 290R

Affected site:

Position: 290
Residue: R
Type: methylation

Impact:

distal

Other known mutations affecting this site

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Mutation
In sequence
Distance
Impact
290L RTEEENL[R/L]RKKGEPHH 0
direct
290P RTEEENL[R/P]RKKGEPHH 0
direct
290H RTEEENL[R/H]RKKGEPHH 0
direct
290C RTEEENL[R/C]RKKGEPHH 0
direct
290G RTEEENL[R/G]RKKGEPHH 0
direct
Showing 1 to 5 of 31 rows

PTM Site: 291K

Affected site:

Position: 291
Residue: K
Type: ubiquitination

Impact:

distal

Other known mutations affecting this site

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Mutation
In sequence
Distance
Impact
291N TEEENLR[K/N]KKGEPHHE 0
direct
291E TEEENLR[K/E]KKGEPHHE 0
direct
292I TEEENLRK[K/I]KGEPHHE 1
proximal
292R TEEENLRK[K/R]KGEPHHE 1
proximal
290L TEEENL[R/L]RKKGEPHHE 1
proximal
Showing 1 to 5 of 29 rows

External references

dbSNP:

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