C136640Level 7
Non-synonymous STAT Family Gene Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A point mutation in a gene that is a member of the STAT gene family that encodes an amino acid substitution in a STAT family protein.
**Synonyms:** - Non-synonymous Signal Transducer and Activator of Transcription Family Gene Mutation - STAT Family Gene Missense Mutation
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