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Summary

Isoform:
Position:
37
Ref:
A
Mutation:
V
PTM impact:
distal
PTM affected:
3
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

LUAD

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

Hereditary nonpolyposis colorectal neoplasms

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 41S

External references

dbSNP:

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