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Summary

Isoform:
Position:
702
Ref:
S
Mutation:
T
PTM impact:
none
PTM affected:
0
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

HNSC

Cancer types: (PCAWG)

Head-SCC

Disease Annotations: (ClinVar)

no data

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

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