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Mutation:
NCKAP1 I137S
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
[0.0199681]
PTM Site: 142T
Affected site:
Position: 142
Residue: T
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 137S | DL[I/S]IITYTTLMILLSR | 5 |
distal
|
| 141R | DLIITY[T/R]TTLMILLSR | 1 |
proximal
|
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