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Mutation:
ISOC2 M1K
Summary
Clinical Information
Cancer types: (TCGA MC3)
UCEC
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: 7S
Affected site:
Position: 7
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 10Q | -MAAARPSLG[R/Q]RVLPG | 3 |
distal
|
| 7R | -MAAARP[S/R]SLGRVLPG | 0 |
direct
|
| 2V | -M[A/V]AAARPSLGRVLPG | 5 |
distal
|
| 1K | -[M/K]MAAARPSLGRVLPG | 6 |
distal
|
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