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Mutation:
SEMA3F G488R
Summary
Clinical Information
Cancer types: (TCGA MC3)
STAD
Cancer types: (PCAWG)
Lymph-BNHL
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 485T
Affected site:
Position: 485
Residue: T
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
487H | YEVLFLGTD[R/H]RGTVQK | 2 |
network-rewiring
|
479K | Y[E/K]EVLFLGTDRGTVQK | 6 |
distal
|
488R | YEVLFLGTDR[G/R]GTVQK | 3 |
distal
|
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