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Mutation:
KAT7 S50I
Summary
Clinical Information
Cancer types: (TCGA MC3)
COAD
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 45S
Affected site:
Position: 45
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 46L | RSARVTRS[S/L]SARLSQS | 1 |
proximal
|
| 44C | RSARVT[R/C]RSSARLSQS | 1 |
proximal
|
| 50I | RSARVTRSSARL[S/I]SQS | 5 |
distal
|
| 41Q | RSA[R/Q]RVTRSSARLSQS | 4 |
distal
|
PTM Site: 46S
Affected site:
Position: 46
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 46L | SARVTRS[S/L]SARLSQSS | 0 |
direct
|
| 44C | SARVT[R/C]RSSARLSQSS | 2 |
proximal
|
| 50I | SARVTRSSARL[S/I]SQSS | 4 |
distal
|
| 41Q | SA[R/Q]RVTRSSARLSQSS | 5 |
distal
|
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