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Summary

Isoform:
Position:
337
Ref:
R
Mutation:
L
PTM impact:
direct
PTM affected:
3
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

LUAD, LUSC, HNSC, COAD, SARC

Cancer types: (PCAWG)

Lung-SCC, Eso-AdenoCa, Bone-Leiomyo, Liver-HCC

Disease Annotations: (ClinVar)

Hereditary cancer-predisposing syndrome

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

External references

dbSNP:

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