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C184317Level 7

Monoallelic RAD51B Gene Inactivation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** Any gain, loss, or exchange of DNA that results in monoallelic loss of function mutations in the RAD51B gene.

**Synonyms:** - Monoallelic Inactivating RAD51B Gene Mutation - Monoallelic Inactivating RAD51B Mutation - Monoallelic R51H2 Gene Inactivation - Monoallelic RAD51 Paralog B Gene Inactivation - Monoallelic RAD51B Inactivating Gene Mutation - Monoallelic RAD51B Inactivating Mutation - Monoallelic RAD51B Inactivation - Monoallelic RAD51B Loss of Function - Monoallelic RAD51B Loss of Function Gene Mutation - Monoallelic RAD51B Loss of Function Mutation - Monoallelic RAD51L1 Gene Inactivation - Monoallelic REC2 Gene Inactivation - RAD51B Gene LOH - RAD51B Homozygous Loss - RAD51B Loss of Heterozygosity

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