Mosaic Mutants

Genetics are very complicated. There are so many factors that influence how we become who we are on the cellular level and beyond.

A good friend of mine always points out- there are many ways to make a family. Those of us in the support group learned that as we have become a family of misfit mutants. Yet even within our small numbers, there are the rare of the rare. I remember at the conference in Boston, talks turned to questions over the topic of mosaicism. There is no easy way to explain it, understand it or definitively peg it’s role in how Li-Fraumeni Syndrome is inherited or develops. We, as mutants are pretty used to chartering uncharted territories- so let’s give it a shot!

Art by Inge Vandormael. Coloring by Bella. Not all cells may have the TP53 mutation. Mosaicism is one of these cases.


Pretty tile murals? How I would like to tile the swimming pool I have in my dream home? Where a person has cells of different genetic make up? Yep, that is the one.

Genetic Mosaicism starts in the GERM cells (eggs and sperm).  It often is silent, meaning the mutation is there, but doesn’t produce the effect (cancer, in the case of LFS) in the person.  As the cells divide during pregnancy, a zygote (little pre-baby alien conglomerate of cells) forms and sometimes a mutation occurs. Depending on where and when this mutation occurs, this affects what percentage of all cells are mutated, and how many are mutated. If the mutation is early in development, many cells will be affected, if the mutation occurs later, fewer cells are affected.

So if a person has a TP53 mosaic mutation, some tissues (for example, it could be just skin, ovaries and breasts) may have the mutated gene, while others do not. The tissues that have the mutation will have a greater risk of developing cancer because p53’s job is to help suppress tumors, and mutant p53 doesn’t always do this properly.

Here is Wendy Kohlmann, MS, CGC, a licensed genetic counselor at the University of Utah Huntsman Cancer Institute, explaining mosaicism to LLFS board member Andi Last for the Learning Li-Fraumeni Syndrome podcast:


Generally, LFS is already on the doc’s radar if you’ve been referred for genetic testing. These times are where Geneticists and Genetic Counselors are worth their weight in gold! To test for LFS, we test for the TP53 mutation while considering family history.

Testing for TP53 mutations can be done several ways, but usually by blood test. If there is a known mutation in a family, they test for that mutation. If there is not, they do a multi-gene sequencing panel to try and find a mutation.  The blood can have cells with different chromosome make up, but this isn’t always the case. If the mutation is in the blood, there will be a certain percentage of changes.

To truly understand where the mutation is, we would have to test all the different cells in the body. That it a daunting and seemingly painful task. This is where the knowledgeable genetic professional becomes a HUGE asset. A geneticist will be able to help determine what testing is necessary and how to go about it for diagnosis.


Right, so here you are in the LFS club. Rarest of the Rare. You have an increased risk of cancer, you just don’t know where or when. No one with LFS knows. That’s why we screen. The benefit to identifying mosaicism is knowing that there is an increased risk, and you can potentially pass along the mutation to your children. Since people with mosaicism have fewer cells affected by the mutation, they tend to have less severe cases of LFS.

That’s not particularly helpful as far as screening goes, unless you know which tissues are affected. We can not yet predict how a mosaic TP53 mutation will affect mutants. But guess what? We can’t predict yet how a non-mosaic TP53 mutation will affect mutants either. Having an increased risk of cancer sucks, no matter what way you slice it.  This is why paying attention you your body, your gut and having a dedicated team will help you navigate these shark-infested waters.

Living LFS is a balance of advocacy and knowledge. Being rare does not mean you cannot get the best care – it means you are human. We are each unique. By knowing we have a rare mutation, we can do our best to fight cancer in a way our bodies can handle. Knowing what you are up against is your best chance at preparing.

Variants of Uncertain Significance(VUS) in LFS

Few things are more frustrating than looking for answers and getting the response- we don’t know. Sometimes, a person agonizes over the decision to be tested for a hereditary cancer syndrome like LFS, finally getting tested just to know for sure. Unfortunately the results aren’t always a clear cut; Yes, you have LFS or No, you do not have LFS.

There are thousands and thousands of changes that can occur to our DNA, called mutations. Not all mutations are harmful- whether or not the mutations are “bad” is a personal opinion. There are mutations that we just don’t know if they are harmful or harmless, in the case of LFS, we don’t know if the mutation is associated with cancer.  They are called Variants of Uncertain Significance (VUS),  also known as Variants of Unknown Significance (still VUS), or  Unclassified Variants.


Li-Fraumeni Syndrome is associated with mutations in the TP53 gene. TP53 makes a tumor suppressor, so if the tumor suppressor doesn’t work right, we sprout tumors. There are many spots on the DNA, where mutations can occur. Some change the way the gene works, some do not. Sometimes the gene only works a little bit.  For more reading on mutations and how they affect us, you can read our blog “Some MUTATIONS are NONSENSE“.

When classifying variants (changes in DNA/mutations) there is a scale from 1-5 – Benign to Pathogenic. Benign (B9 to experienced mutants) means not harmful or more importantly not malignant. Pathogenic means to cause a disease- in our case, cancers.

  1. Benign means there is no change caused by the variant.
  2. Likely Benign means suspected to not cause disease.
  3. Uncertain are VUS (Variants of Uncertain Significance) this means there is not enough data to know if the mutation will cause disease or not.
  4. Likely Pathogenic means the variant is suspected to cause disease.
  5. Pathogenic means the variant is known to cause disease.


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Genomic Variant Scale from

The American Society of Human Genetics (ASHG) advises that VUS should not be used for decision making, they are neither good nor bad, and all medical decisions should be based on medical findings and family history. This does not mean you are negative for a mutation, it simply means there is a mutation there and that we do not have enough information to momentarily identify what the risk is. The best bet is to consult with a trusted geneticist or genetic counselor ( to evaluate your risk based on what you do know – your medical history, your family history, and other relevant factors.

Things to Remember:

You cannot interpret what is not known. Li-Fraumeni Syndrome is rare, we just don’t have the research numbers to know if VUS are linked to cancers. Not everyone with LFS linked mutations get cancer. We know some mutations are linked to certain cancers in LFS but there is still a lot of uncertainty. Participating in studies, such as PROMPT help record data and could help predict if certain VUS might be linked to risk of certain cancers or not.

Focus on what you can control. You can control diet, exercise, and other contributing factors to a healthy lifestyle. Although we can not control mutations, we can try to reduce our risk. A genetic counselor can help you evaluate risk and decide what and if a screening regimen would be good for you. Many people with LFS follow the Toronto Protocol, however, the best regimen is the one that works best for you, your risk, insurance coverage, and lifestyle.

As we learn more, classifications can change. When TP53 was first discovered, it was thought to be an oncogene, a gene that causes cancer. After decades of research, it was reclassified as a tumor suppressor gene. Keeping up with current research can help you advocate for yourself and live LFS.

LLFS Board Member Andi connected with Wendy Kohlmann, MS, CGC, a licensed genetic counselor at the University of Utah Huntsman Cancer Institute. In this excerpt from her interview for the Learning Li-Fraumeni Syndrome podcast, she explains what it means when your genetic test results show a VUS: a variant of uncertain significance or variant of unknown significance.

Resources and more reading on VUS:

American Society of Human Genetics on VUS

Mayo Clinic pdf on VUS

Think Genetic LFS VUS