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Summary

Isoform:
Position:
506
Ref:
E
Mutation:
D
PTM impact:
distal
PTM affected:
2
Kinases:
CDK2

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

no data

Minor Allele Frequency: (ESP6500)

[0.0077]

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 499S

Affected site:

Position: 499
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
505R PPCLENSSPPSRI[P/R]PE 6
distal
505S PPCLENSSPPSRI[P/S]PE 6
distal
494Y PP[C/Y]CLENSSPPSRIPE 5
distal
493L P[P/L]PCLENSSPPSRIPE 6
distal
505L PPCLENSSPPSRI[P/L]PE 6
distal
505A PPCLENSSPPSRI[P/A]PE 6
distal

PTM Site: 509S

Affected site:

Position: 509
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
514D SRIPEPESPAKP[N/D]NVP 5
distal
511V SRIPEPESP[A/V]AKPNVP 2
proximal
506D SRIP[E/D]EPESPAKPNVP 3
distal
505R SRI[P/R]PEPESPAKPNVP 4
distal
505S SRI[P/S]PEPESPAKPNVP 4
distal
505L SRI[P/L]PEPESPAKPNVP 4
distal
505A SRI[P/A]PEPESPAKPNVP 4
distal
507L SRIPE[P/L]PESPAKPNVP 2
proximal

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