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Mutation:
PALLD T43S
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
Pancreatic cancer 1
Minor Allele Frequency: (ESP6500)
[0.4075]
Minor Allele Frequency: (1000 Genomes)
[0.09984029999999999]
PTM Site: 41S
Affected site:
Position: 41
Residue: S
Type: phosphorylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 43S | VPVQQVHSP[T/S]TSYLCR | 2 |
proximal
|
| 43N | VPVQQVHSP[T/N]TSYLCR | 2 |
proximal
|
| 40Q | VPVQQV[H/Q]HSPTSYLCR | 1 |
proximal
|
| 46I | VPVQQVHSPTSY[L/I]LCR | 5 |
distal
|
External references
dbSNP:
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