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Summary

Isoform:
Position:
26
Ref:
L
Mutation:
I
PTM impact:
proximal
PTM affected:
3
Kinases:
ATR, PRKDC, CSNK1D, PLK3, PRKAA1, MAPK8, CSNK1A1, DAPK3, CHEK1, ATM, CHK2, CDK5, STK17A, MAPK9, CHEK2, CHK1, DAPK1, MAPKAPK2, CDK group, GSK-3 group, PRKDC, CDK9, MAPK12, ATM, CDK7, MAPK14, GSK3B, CDK5

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

Hereditary cancer-predisposing syndrome

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 20S

Affected site:

Position: 20
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
26I PLSQETFSDLWKL[L/I]LP 6
distal
20L PLSQETF[S/L]SDLWKLLP 0
direct
20P PLSQETF[S/P]SDLWKLLP 0
direct
16H PLS[Q/H]QETFSDLWKLLP 4
distal
16R PLS[Q/R]QETFSDLWKLLP 4
distal
14V P[L/V]LSQETFSDLWKLLP 6
distal

PTM Site: 24K

Affected site:

Position: 24
Residue: K
Type: ubiquitination

Impact:

proximal

PTM Site: 33S

Affected site:

Position: 33
Residue: S
Type: phosphorylation

Impact:

distal

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