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Summary

Isoform:
Position:
61
Ref:
Y
Mutation:
H
PTM impact:
direct
PTM affected:
3
Kinases:
AURKA, AURORA A, PAK4, AURKB, SRC

Clinical Information

Cancer types: (TCGA MC3)

BRCA, LGG, SARC, CESC

Cancer types: (PCAWG)

Breast-AdenoCa

Disease Annotations: (ClinVar)

Hereditary cancer-predisposing syndrome, Li-Fraumeni syndrome

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

[0.0199681]

PTM Site: 54R

Affected site:

Position: 54
Residue: R
Type: methylation

Impact:

distal

Other known mutations affecting this site

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Mutation
In sequence
Distance
Impact
54L LDDRNTF[R/L]RHSVVVPY 0
direct
54P LDDRNTF[R/P]RHSVVVPY 0
direct
54Q LDDRNTF[R/Q]RHSVVVPY 0
direct
54G LDDRNTF[R/G]RHSVVVPY 0
direct
55Q LDDRNTFR[H/Q]HSVVVPY 1
proximal
Showing 1 to 5 of 38 rows

PTM Site: 56S

Affected site:

Position: 56
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

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Mutation
In sequence
Distance
Impact
56R DRNTFRH[S/R]SVVVPYEP 0
direct
56I DRNTFRH[S/I]SVVVPYEP 0
direct
56T DRNTFRH[S/T]SVVVPYEP 0
direct
56N DRNTFRH[S/N]SVVVPYEP 0
direct
56G DRNTFRH[S/G]SVVVPYEP 0
direct
Showing 1 to 5 of 41 rows

PTM Site: 61Y

Affected site:

Position: 61
Residue: Y
Type: phosphorylation

Impact:

direct

Other known mutations affecting this site

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Mutation
In sequence
Distance
Impact
61C RHSVVVP[Y/C]YEPPEVGS 0
direct
61S RHSVVVP[Y/S]YEPPEVGS 0
direct
61D RHSVVVP[Y/D]YEPPEVGS 0
direct
61H RHSVVVP[Y/H]YEPPEVGS 0
direct
61N RHSVVVP[Y/N]YEPPEVGS 0
direct
Showing 1 to 5 of 42 rows

External references

dbSNP:

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