|
|
| Line 88: |
Line 88: |
| ==Characteristic Chromosomal or Other Global Mutational Patterns== | | ==Characteristic Chromosomal or Other Global Mutational Patterns== |
|
| |
|
| | | N/A |
| Put your text here and fill in the table <span style="color:#0070C0">(I''nstructions: Included in this category are alterations such as hyperdiploid; gain of odd number chromosomes including typically chromosome 1, 3, 5, 7, 11, and 17; co-deletion of 1p and 19q; complex karyotypes without characteristic genetic findings; chromothripsis; microsatellite instability; homologous recombination deficiency; mutational signature pattern; etc. Details on clinical significance such as prognosis and other important information can be provided in the notes section. Please include references throughout the table. Do not delete the table.'')</span>
| |
| {| class="wikitable sortable" | | {| class="wikitable sortable" |
| |- | | |- |
| Line 124: |
Line 123: |
| |} | | |} |
|
| |
|
| <blockquote class="blockedit">{{Box-round|title=v4:Characteristic Chromosomal Aberrations / Patterns|The content below was from the old template. Please incorporate above.}}</blockquote>
| | == Gene Mutations (SNV/INDELS) == |
| | | <center> |
| | |
| *<blockquote class="blockedit">
| |
| <center><span style="color:Maroon">'''End of V4 Section'''</span>
| |
| ----
| |
| <blockquote class="blockedit">
| |
| <center><span style="color:Maroon">'''End of V4 Section'''</span>
| |
| ----
| |
| </blockquote>
| |
| </blockquote>
| |
| ==Gene Mutations (SNV/INDEL)== | |
| | |
| * Somatic mutations have been reported; however, consistent/recurrent mutations are not well-described.<ref name=":10" /> | | * Somatic mutations have been reported; however, consistent/recurrent mutations are not well-described.<ref name=":10" /> |
| ** Rare reports of mutations in FYN<ref name=":10" />,
| |
|
| |
|
| | * Rare reports of mutations in FYN<ref name=":10" />, |
| {| class="wikitable sortable" | | {| class="wikitable sortable" |
| |- | | |- |
