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Mutation:
SERPINB12 M41I
Summary
Clinical Information
Cancer types: (TCGA MC3)
LUSC
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: 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
|
PTM Site: 36S
Affected site:
Position: 36
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
38P | FFSPLSLSA[A/P]ALGMVR | 2 |
proximal
|
34N | FFSPL[S/N]SLSAALGMVR | 2 |
proximal
|
40S | FFSPLSLSAAL[G/S]GMVR | 4 |
distal
|
41I | FFSPLSLSAALG[M/I]MVR | 5 |
distal
|
33P | FFSP[L/P]LSLSAALGMVR | 3 |
distal
|
35P | FFSPLS[L/P]LSAALGMVR | 1 |
proximal
|
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