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| EXAMPLE: | | EXAMPLE: |
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− | * ''TP53'' is a well-described tumor suppressor gene that functions in apoptosis, genomic stability and inhibition of angiogenesis (RefSeq, Dec 2016). | + | *''TP53'' is a well-described tumor suppressor gene that functions in apoptosis, genomic stability and inhibition of angiogenesis (RefSeq, Dec 2016). |
− | * Germline loss-of-function alterations, including deletions, are associated with Li-Fraumeni cancer predisposition syndrome (LFS). Individuals with LFS are at an increased risk of developing cancer, particularly sarcomas (PMID: 20586629, 27621308, 25896519). | + | *Germline loss-of-function alterations, including deletions, are associated with Li-Fraumeni cancer predisposition syndrome (LFS). Individuals with LFS are at an increased risk of developing cancer, particularly sarcomas (PMID: 20586629, 27621308, 25896519). |
− | * Somatic ''TP53'' alterations are reported at a high frequency across a wide range of tumors, arising in ~30% of all cancer patients (PMID: 25400752, 27239089, cbioportal.org accessed 6/2/21). | + | *Somatic ''TP53'' alterations are reported at a high frequency across a wide range of tumors, arising in ~30% of all cancer patients (PMID: 25400752, 27239089, cbioportal.org accessed 6/2/21). |
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| ==Clinical Cancer Associations (Somatic)== | | ==Clinical Cancer Associations (Somatic)== |
| + | (''Instruction: include references and links to related internal CCGA pages'') |
| {| class="wikitable" | | {| class="wikitable" |
| |'''Tumor Type''' | | |'''Tumor Type''' |
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| |'''Therapeutic Significance (Yes, No or Unknown)''' | | |'''Therapeutic Significance (Yes, No or Unknown)''' |
| |- | | |- |
− | |EXAMPLE: Chronic Myeloid Leukemia (CML), BCR-ABL1 Positive (link to internal page through this name) | + | |EXAMPLE: Chronic Myeloid Leukemia (CML), BCR-ABL1 Positive (link this name to internal page using link icon above) |
| |EXAMPLES: Copy Number Loss, Copy Number Gain, LOH, Loss-of-Function Mutation, Gain-of-Function Mutation, Translocation/Fusion, Expression Changes (Biomarker), Somatic Hypermutation | | |EXAMPLES: Copy Number Loss, Copy Number Gain, LOH, Loss-of-Function Mutation, Gain-of-Function Mutation, Translocation/Fusion, Expression Changes (Biomarker), Somatic Hypermutation |
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| ==Clinical Cancer Associations (Germline)== | | ==Clinical Cancer Associations (Germline)== |
| + | (''Instruction: include references and links to related internal CCGA pages'') |
| {| class="wikitable" | | {| class="wikitable" |
| |'''Tumor Type''' | | |'''Tumor Type''' |
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| |'''Therapeutic Significance (Yes, No or Unknown)''' | | |'''Therapeutic Significance (Yes, No or Unknown)''' |
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− | |EXAMPLE: Myeloid Neoplasms with Germline ANKRD26 Mutation (link to internal page through this name) | + | |EXAMPLE: Myeloid Neoplasms with Germline ANKRD26 Mutation (link this name to internal page using link icon above) |
| |EXAMPLES: Copy Number Loss, Copy Number Gain, LOH, Loss-of-Function Mutation, Gain-of-Function Mutation, Translocation/Fusion, | | |EXAMPLES: Copy Number Loss, Copy Number Gain, LOH, Loss-of-Function Mutation, Gain-of-Function Mutation, Translocation/Fusion, |
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