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Mutation:
SERPINB12 I28L
Summary
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: 34S
Affected site:
Position: 34
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 28L | N[I/L]IFFSPLSLSAALGM | 6 |
distal
|
| 38P | NIFFSPLSLSA[A/P]ALGM | 4 |
distal
|
| 34N | NIFFSPL[S/N]SLSAALGM | 0 |
direct
|
| 40S | NIFFSPLSLSAAL[G/S]GM | 6 |
distal
|
| 33P | NIFFSP[L/P]LSLSAALGM | 1 |
proximal
|
| 35P | NIFFSPLS[L/P]LSAALGM | 1 |
network-rewiring
|
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