Changes in 0d95b27: updates

				FL_genes.md
			
          @@ -109,7 +109,6 @@ link-citations: true

           |[HIST1H2BM](HIST1H2BM)|2, aSHM|[Krysiak et al](papers/krysiakRecurrentSomaticMutations2017b)[@krysiakRecurrentSomaticMutations2017b]||

           |[HIST1H3I](HIST1H3I)|2, aSHM|[Krysiak et al](papers/krysiakRecurrentSomaticMutations2017b)[@krysiakRecurrentSomaticMutations2017b]|[@paneaWholeGenomeLandscape2019]|

           |[HLA-B](HLA-B)|2||[@lohrDiscoveryPrioritizationSomatic2012a; @wienandGenomicAnalysesFlowsorted2019b]|

          -|[HNRNPD](HNRNPD)|2|||

           |[IGLL5](IGLL5)|2, aSHM|[Russler et al](papers/russler-germainMutationsAssociatedProgression2023b)[@russler-germainMutationsAssociatedProgression2023b]|[@deschGenotypingCirculatingTumor2020; @paneaWholeGenomeLandscape2019]|

           |[JUP](JUP)|2|[Hubschmann et al](papers/hubschmannMutationalMechanismsShaping2021b)[@hubschmannMutationalMechanismsShaping2021b]||

           |[KIR3DL1](KIR3DL1)|2|[Russler et al](papers/russler-germainMutationsAssociatedProgression2023b)[@russler-germainMutationsAssociatedProgression2023b]||

          @@ -129,7 +128,6 @@ link-citations: true

           |[PRKDC](PRKDC)|2|[Hubschmann et al](papers/hubschmannMutationalMechanismsShaping2021b)[@hubschmannMutationalMechanismsShaping2021b]|[@schmitzGeneticsPathogenesisDiffuse2018a]|

           |[PZP](PZP)|2|[Russler et al](papers/russler-germainMutationsAssociatedProgression2023b)[@russler-germainMutationsAssociatedProgression2023b]||

           |[RBM6](RBM6)|2|[Hubschmann et al](papers/hubschmannMutationalMechanismsShaping2021b)[@hubschmannMutationalMechanismsShaping2021b]||

          -|[SESN1](SESN1)|2|[Oricchio et al](papers/oricchioGeneticEpigeneticInactivation2017b)[@oricchioGeneticEpigeneticInactivation2017b]||

           |[SHROOM3](SHROOM3)|2|[Russler et al](papers/russler-germainMutationsAssociatedProgression2023b)[@russler-germainMutationsAssociatedProgression2023b]||

           |[SRRM2](SRRM2)|2|[Russler et al](papers/russler-germainMutationsAssociatedProgression2023b)[@russler-germainMutationsAssociatedProgression2023b]|[@morinMutationalStructuralAnalysis2013]|

           |[STAB2](STAB2)|2|[Russler et al](papers/russler-germainMutationsAssociatedProgression2023b)[@russler-germainMutationsAssociatedProgression2023b]||

				PMAIP1.md
			
          @@ -1,38 +0,0 @@

          -# PMAIP1

          -

          -## Relevance tier by entity

          -

          -|Entity|Tier|Description                           |

          -|:------:|:----:|--------------------------------------|

          -|![BL](images/icons/BL_tier2.png)    |2   |relevance in BL not firmly established|

          -

          -## Mutation incidence in large patient cohorts (GAMBL reanalysis)

          -

          -|Entity|source               |frequency (%)|

          -|:------:|:---------------------:|:-------------:|

          -|BL    |GAMBL genomes+capture|3.23         |

          -|BL    |Thomas cohort        |3.00         |

          -|BL    |Panea cohort         |5.00         |

          -

          -## Mutation pattern and selective pressure estimates

          -

          -|Entity|aSHM|Significant selection|dN/dS (missense)|dN/dS (nonsense)|

          -|:------:|:----:|:---------------------:|:----------------:|:----------------:|

          -|BL    |No  |Yes                  |15.382          |90.742          |

          -|DLBCL |No  |No                   | 0.000          | 0.000          |

          -|FL    |No  |No                   | 0.000          | 0.000          |

          -

          -

          -

          -View coding variants in ProteinPaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/PMAIP1_protein.html)  or [hg38](https://morinlab.github.io/LLMPP/GAMBL/PMAIP1_protein_hg38.html)

          -

          -![image](images/proteinpaint/PMAIP1_NM_021127.svg)

          -

          -View all variants in GenomePaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/PMAIP1.html)  or [hg38](https://morinlab.github.io/LLMPP/GAMBL/PMAIP1_hg38.html)

          -

          -![image](images/proteinpaint/PMAIP1.svg)

          -## PMAIP1 Expression

          -![image](images/gene_expression/PMAIP1_by_pathology.svg)

          -<!-- ORIGIN:  -->

          -<!-- BL: 2 -->

          -## References

				SEPT10.md
			
          @@ -1,37 +0,0 @@

          -# SEPT10

          -

          -## Relevance tier by entity

          -

          -|Entity|Tier|Description                           |

          -|:------:|:----:|--------------------------------------|

          -|![BL](images/icons/BL_tier2.png)    |2   |relevance in BL not firmly established|

          -

          -## Mutation incidence in large patient cohorts (GAMBL reanalysis)

          -

          -|Entity|source               |frequency (%)|

          -|:------:|:---------------------:|:-------------:|

          -|BL    |GAMBL genomes+capture|0.92         |

          -|BL    |Thomas cohort        |2.10         |

          -|BL    |Panea cohort         |2.00         |

          -

          -## Mutation pattern and selective pressure estimates

          -

          -|Entity|aSHM|Significant selection|dN/dS (missense)|dN/dS (nonsense)|

          -|:------:|:----:|:---------------------:|:----------------:|:----------------:|

          -|BL    |No  |No                   |7.224           |13.447          |

          -|DLBCL |No  |No                   |0.000           | 0.000          |

          -|FL    |No  |No                   |2.834           | 0.000          |

          -

          -

          -

          -View coding variants in ProteinPaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/SEPT10_protein.html)  or [hg38](https://morinlab.github.io/LLMPP/GAMBL/SEPT10_protein_hg38.html)

          -

          -![image](images/proteinpaint/SEPT10_NM_144710.svg)

          -

          -View all variants in GenomePaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/SEPT10.html)  or [hg38](https://morinlab.github.io/LLMPP/GAMBL/SEPT10_hg38.html)

          -

          -![image](images/proteinpaint/SEPT10.svg)

          -## SEPT10 Expression

          -![image](images/gene_expression/SEPT10_by_pathology.svg)

          -<!-- ORIGIN:  -->

          -<!-- BL: 2 -->

				SESN1.md
			
          @@ -1,44 +0,0 @@

          ----

          -bibliography: 'morinlab.bib'

          -csl: 'NLM.csl'

          -link-citations: true

          ----

          -# SESN1

          -

          -## Relevance tier by entity

          -

          -|Entity|Tier|Description                           |

          -|:------:|:----:|--------------------------------------|

          -|![FL](images/icons/FL_tier2.png)    |2   |relevance in FL not firmly established[@oricchioGeneticEpigeneticInactivation2017b]|

          -

          -## Mutation incidence in large patient cohorts (GAMBL reanalysis)

          -

          -|Entity|source       |frequency (%)|

          -|:------:|:-------------:|:-------------:|

          -|FL    |GAMBL genomes|0.23         |

          -

          -## Mutation pattern and selective pressure estimates

          -

          -|Entity|aSHM|Significant selection|dN/dS (missense)|dN/dS (nonsense)|

          -|:------:|:----:|:---------------------:|:----------------:|:----------------:|

          -|BL    |No  |No                   |4.805           |0               |

          -|DLBCL |No  |No                   |1.629           |0               |

          -|FL    |No  |No                   |0.000           |0               |

          -

          -

          -

          -

          -View coding variants in ProteinPaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/SESN1_protein.html)  or [hg38](https://morinlab.github.io/LLMPP/GAMBL/SESN1_protein_hg38.html)

          -

          -![](images/proteinpaint/SESN1_NM_014454.svg)

          -

          -View all variants in GenomePaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/SESN1.html)  or [hg38](https://morinlab.github.io/LLMPP/GAMBL/SESN1_hg38.html)

          -

          -![](images/proteinpaint/SESN1.svg)

          -

          -## SESN1 Expression

          -![](images/gene_expression/SESN1_by_pathology.svg)

          -<!-- ORIGIN: oricchioGeneticEpigeneticInactivation2017b -->

          -

          -## References

          -<!-- FL: oricchioGeneticEpigeneticInactivation2017b -->

				SYNCRIP.md
			
          @@ -1,49 +0,0 @@

          -# SYNCRIP

          -

          -## History

          -```mermaid

          -%%{init: { 'logLevel': 'debug', 'theme': 'dark' } }%%

          -timeline

          -    title Publication timing

          -      2019-09-26 : Panea : BL

          -```

          -

          -## Relevance tier by entity

          -

          -|Entity|Tier|Description                           |

          -|:------:|:----:|--------------------------------------|

          -|![BL](images/icons/BL_tier2.png)    |2   |relevance in BL not firmly established|

          -

          -## Mutation incidence in large patient cohorts (GAMBL reanalysis)

          -

          -|Entity|source               |frequency (%)|

          -|:------:|:---------------------:|:-------------:|

          -|BL    |GAMBL genomes+capture|3.0          |

          -|BL    |Thomas cohort        |2.5          |

          -|BL    |Panea cohort         |5.0          |

          -

          -## Mutation pattern and selective pressure estimates

          -

          -|Entity|aSHM|Significant selection|dN/dS (missense)|dN/dS (nonsense)|

          -|:------:|:----:|:---------------------:|:----------------:|:----------------:|

          -|BL    |No  |No                   | 4.806          |35.301          |

          -|DLBCL |No  |No                   | 2.325          |47.239          |

          -|FL    |No  |No                   |16.820          | 0.000          |

          -

          -

          -

          -View coding variants in ProteinPaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/SYNCRIP_protein.html)  or [hg38](https://morinlab.github.io/LLMPP/GAMBL/SYNCRIP_protein_hg38.html)

          -

          -![](images/proteinpaint/SYNCRIP_NM_006372.svg)

          -

          -View all variants in GenomePaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/SYNCRIP.html)  or [hg38](https://morinlab.github.io/LLMPP/GAMBL/SYNCRIP_hg38.html)

          -

          -![](images/proteinpaint/SYNCRIP.svg)

          -

          -## SYNCRIP Expression

          -![](images/gene_expression/SYNCRIP_by_pathology.svg)

          -<!-- ORIGIN: paneaWholeGenomeLandscape2019 -->

          -<!-- BL: paneaWholeGenomeLandscape2019 -->

          -

          -## References

          -1.  Panea R, Love C, Shingleton JR, Reddy A, Bailey J, Moormann A, Otieno J, Ong’echa J, Oduor C, Schroêder K, Masalu N, Chao N, Agajanian M, Major M, Fedoriw Y, Richards K, Rymkiewicz G, Miles R, Alobeid B, Bhagat G, Flowers C, Ondrejka S, Hsi E, Choi W, Au-Yeung R, Hartmann W, Lenz G, Meyerson H, Lin YY, Zhuang Y, Luftig M, Waldrop A, Dave T, Thakkar D, Sahay H, Li G, Palus B, Seshadri V, Kim S, Gascoyne R, Levy S, Mukhopadhyay M, Dunson D, Dave S. The whole genome landscape of Burkitt lymphoma subtypes. Blood. 2019;

				all_entities.md
			
          @@ -509,7 +509,6 @@

           |[SENP7](SENP7)|||||![PMBL](images/icons/PMBL_tier2.png)||

           |[SEPTIN9](SEPTIN9)||![DLBCL](images/icons/DLBCL_tier2.png)|||||

           |[SERPINA9](SERPINA9)||![DLBCL](images/icons/DLBCL_tier2.png)|||||

          -|[SESN1](SESN1)|![FL](images/icons/FL_tier2.png)||||||

           |[SETD1B](SETD1B)||![DLBCL](images/icons/DLBCL_tier1.png)|||||

           |[SETD2](SETD2)||![DLBCL](images/icons/DLBCL_tier2.png)|||||

           |[SETD5](SETD5)||![DLBCL](images/icons/DLBCL_tier2.png)|||![PMBL](images/icons/PMBL_tier2.png)||

...	...	@@ -509,7 +509,6 @@
509	509	\|[SENP7](SENP7)\|\|\|\|\|![PMBL](images/icons/PMBL_tier2.png)\|\|
510	510	\|[SEPTIN9](SEPTIN9)\|\|![DLBCL](images/icons/DLBCL_tier2.png)\|\|\|\|\|
511	511	\|[SERPINA9](SERPINA9)\|\|![DLBCL](images/icons/DLBCL_tier2.png)\|\|\|\|\|
512		-\|[SESN1](SESN1)\|![FL](images/icons/FL_tier2.png)\|\|\|\|\|\|
513	512	\|[SETD1B](SETD1B)\|\|![DLBCL](images/icons/DLBCL_tier1.png)\|\|\|\|\|
514	513	\|[SETD2](SETD2)\|\|![DLBCL](images/icons/DLBCL_tier2.png)\|\|\|\|\|
515	514	\|[SETD5](SETD5)\|\|![DLBCL](images/icons/DLBCL_tier2.png)\|\|\|![PMBL](images/icons/PMBL_tier2.png)\|\|

...	...	@@ -109,7 +109,6 @@ link-citations: true
109	109	\|[HIST1H2BM](HIST1H2BM)\|2, aSHM\|[Krysiak et al](papers/krysiakRecurrentSomaticMutations2017b)[@krysiakRecurrentSomaticMutations2017b]\|\|
110	110	\|[HIST1H3I](HIST1H3I)\|2, aSHM\|[Krysiak et al](papers/krysiakRecurrentSomaticMutations2017b)[@krysiakRecurrentSomaticMutations2017b]\|[@paneaWholeGenomeLandscape2019]\|
111	111	\|[HLA-B](HLA-B)\|2\|\|[@lohrDiscoveryPrioritizationSomatic2012a; @wienandGenomicAnalysesFlowsorted2019b]\|
112		-\|[HNRNPD](HNRNPD)\|2\|\|\|
113	112	\|[IGLL5](IGLL5)\|2, aSHM\|[Russler et al](papers/russler-germainMutationsAssociatedProgression2023b)[@russler-germainMutationsAssociatedProgression2023b]\|[@deschGenotypingCirculatingTumor2020; @paneaWholeGenomeLandscape2019]\|
114	113	\|[JUP](JUP)\|2\|[Hubschmann et al](papers/hubschmannMutationalMechanismsShaping2021b)[@hubschmannMutationalMechanismsShaping2021b]\|\|
115	114	\|[KIR3DL1](KIR3DL1)\|2\|[Russler et al](papers/russler-germainMutationsAssociatedProgression2023b)[@russler-germainMutationsAssociatedProgression2023b]\|\|
...	...	@@ -129,7 +128,6 @@ link-citations: true
129	128	\|[PRKDC](PRKDC)\|2\|[Hubschmann et al](papers/hubschmannMutationalMechanismsShaping2021b)[@hubschmannMutationalMechanismsShaping2021b]\|[@schmitzGeneticsPathogenesisDiffuse2018a]\|
130	129	\|[PZP](PZP)\|2\|[Russler et al](papers/russler-germainMutationsAssociatedProgression2023b)[@russler-germainMutationsAssociatedProgression2023b]\|\|
131	130	\|[RBM6](RBM6)\|2\|[Hubschmann et al](papers/hubschmannMutationalMechanismsShaping2021b)[@hubschmannMutationalMechanismsShaping2021b]\|\|
132		-\|[SESN1](SESN1)\|2\|[Oricchio et al](papers/oricchioGeneticEpigeneticInactivation2017b)[@oricchioGeneticEpigeneticInactivation2017b]\|\|
133	131	\|[SHROOM3](SHROOM3)\|2\|[Russler et al](papers/russler-germainMutationsAssociatedProgression2023b)[@russler-germainMutationsAssociatedProgression2023b]\|\|
134	132	\|[SRRM2](SRRM2)\|2\|[Russler et al](papers/russler-germainMutationsAssociatedProgression2023b)[@russler-germainMutationsAssociatedProgression2023b]\|[@morinMutationalStructuralAnalysis2013]\|
135	133	\|[STAB2](STAB2)\|2\|[Russler et al](papers/russler-germainMutationsAssociatedProgression2023b)[@russler-germainMutationsAssociatedProgression2023b]\|\|

...	...	@@ -1,38 +0,0 @@
1		-# PMAIP1
2		-
3		-## Relevance tier by entity
4		-
5		-\|Entity\|Tier\|Description \|
6		-\|:------:\|:----:\|--------------------------------------\|
7		-\|![BL](images/icons/BL_tier2.png) \|2 \|relevance in BL not firmly established\|
8		-
9		-## Mutation incidence in large patient cohorts (GAMBL reanalysis)
10		-
11		-\|Entity\|source \|frequency (%)\|
12		-\|:------:\|:---------------------:\|:-------------:\|
13		-\|BL \|GAMBL genomes+capture\|3.23 \|
14		-\|BL \|Thomas cohort \|3.00 \|
15		-\|BL \|Panea cohort \|5.00 \|
16		-
17		-## Mutation pattern and selective pressure estimates
18		-
19		-\|Entity\|aSHM\|Significant selection\|dN/dS (missense)\|dN/dS (nonsense)\|
20		-\|:------:\|:----:\|:---------------------:\|:----------------:\|:----------------:\|
21		-\|BL \|No \|Yes \|15.382 \|90.742 \|
22		-\|DLBCL \|No \|No \| 0.000 \| 0.000 \|
23		-\|FL \|No \|No \| 0.000 \| 0.000 \|
24		-
25		-
26		-
27		-View coding variants in ProteinPaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/PMAIP1_protein.html) or [hg38](https://morinlab.github.io/LLMPP/GAMBL/PMAIP1_protein_hg38.html)
28		-
29		-![image](images/proteinpaint/PMAIP1_NM_021127.svg)
30		-
31		-View all variants in GenomePaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/PMAIP1.html) or [hg38](https://morinlab.github.io/LLMPP/GAMBL/PMAIP1_hg38.html)
32		-
33		-![image](images/proteinpaint/PMAIP1.svg)
34		-## PMAIP1 Expression
35		-![image](images/gene_expression/PMAIP1_by_pathology.svg)
36		-<!-- ORIGIN: -->
37		-<!-- BL: 2 -->
38		-## References

...	...	@@ -1,37 +0,0 @@
1		-# SEPT10
2		-
3		-## Relevance tier by entity
4		-
5		-\|Entity\|Tier\|Description \|
6		-\|:------:\|:----:\|--------------------------------------\|
7		-\|![BL](images/icons/BL_tier2.png) \|2 \|relevance in BL not firmly established\|
8		-
9		-## Mutation incidence in large patient cohorts (GAMBL reanalysis)
10		-
11		-\|Entity\|source \|frequency (%)\|
12		-\|:------:\|:---------------------:\|:-------------:\|
13		-\|BL \|GAMBL genomes+capture\|0.92 \|
14		-\|BL \|Thomas cohort \|2.10 \|
15		-\|BL \|Panea cohort \|2.00 \|
16		-
17		-## Mutation pattern and selective pressure estimates
18		-
19		-\|Entity\|aSHM\|Significant selection\|dN/dS (missense)\|dN/dS (nonsense)\|
20		-\|:------:\|:----:\|:---------------------:\|:----------------:\|:----------------:\|
21		-\|BL \|No \|No \|7.224 \|13.447 \|
22		-\|DLBCL \|No \|No \|0.000 \| 0.000 \|
23		-\|FL \|No \|No \|2.834 \| 0.000 \|
24		-
25		-
26		-
27		-View coding variants in ProteinPaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/SEPT10_protein.html) or [hg38](https://morinlab.github.io/LLMPP/GAMBL/SEPT10_protein_hg38.html)
28		-
29		-![image](images/proteinpaint/SEPT10_NM_144710.svg)
30		-
31		-View all variants in GenomePaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/SEPT10.html) or [hg38](https://morinlab.github.io/LLMPP/GAMBL/SEPT10_hg38.html)
32		-
33		-![image](images/proteinpaint/SEPT10.svg)
34		-## SEPT10 Expression
35		-![image](images/gene_expression/SEPT10_by_pathology.svg)
36		-<!-- ORIGIN: -->
37		-<!-- BL: 2 -->

...	...	@@ -1,44 +0,0 @@
1		----
2		-bibliography: 'morinlab.bib'
3		-csl: 'NLM.csl'
4		-link-citations: true
5		----
6		-# SESN1
7		-
8		-## Relevance tier by entity
9		-
10		-\|Entity\|Tier\|Description \|
11		-\|:------:\|:----:\|--------------------------------------\|
12		-\|![FL](images/icons/FL_tier2.png) \|2 \|relevance in FL not firmly established[@oricchioGeneticEpigeneticInactivation2017b]\|
13		-
14		-## Mutation incidence in large patient cohorts (GAMBL reanalysis)
15		-
16		-\|Entity\|source \|frequency (%)\|
17		-\|:------:\|:-------------:\|:-------------:\|
18		-\|FL \|GAMBL genomes\|0.23 \|
19		-
20		-## Mutation pattern and selective pressure estimates
21		-
22		-\|Entity\|aSHM\|Significant selection\|dN/dS (missense)\|dN/dS (nonsense)\|
23		-\|:------:\|:----:\|:---------------------:\|:----------------:\|:----------------:\|
24		-\|BL \|No \|No \|4.805 \|0 \|
25		-\|DLBCL \|No \|No \|1.629 \|0 \|
26		-\|FL \|No \|No \|0.000 \|0 \|
27		-
28		-
29		-
30		-
31		-View coding variants in ProteinPaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/SESN1_protein.html) or [hg38](https://morinlab.github.io/LLMPP/GAMBL/SESN1_protein_hg38.html)
32		-
33		-![](images/proteinpaint/SESN1_NM_014454.svg)
34		-
35		-View all variants in GenomePaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/SESN1.html) or [hg38](https://morinlab.github.io/LLMPP/GAMBL/SESN1_hg38.html)
36		-
37		-![](images/proteinpaint/SESN1.svg)
38		-
39		-## SESN1 Expression
40		-![](images/gene_expression/SESN1_by_pathology.svg)
41		-<!-- ORIGIN: oricchioGeneticEpigeneticInactivation2017b -->
42		-
43		-## References
44		-<!-- FL: oricchioGeneticEpigeneticInactivation2017b -->

...	...	@@ -1,49 +0,0 @@
1		-# SYNCRIP
2		-
3		-## History
4		-```mermaid
5		-%%{init: { 'logLevel': 'debug', 'theme': 'dark' } }%%
6		-timeline
7		- title Publication timing
8		- 2019-09-26 : Panea : BL
9		-```
10		-
11		-## Relevance tier by entity
12		-
13		-\|Entity\|Tier\|Description \|
14		-\|:------:\|:----:\|--------------------------------------\|
15		-\|![BL](images/icons/BL_tier2.png) \|2 \|relevance in BL not firmly established\|
16		-
17		-## Mutation incidence in large patient cohorts (GAMBL reanalysis)
18		-
19		-\|Entity\|source \|frequency (%)\|
20		-\|:------:\|:---------------------:\|:-------------:\|
21		-\|BL \|GAMBL genomes+capture\|3.0 \|
22		-\|BL \|Thomas cohort \|2.5 \|
23		-\|BL \|Panea cohort \|5.0 \|
24		-
25		-## Mutation pattern and selective pressure estimates
26		-
27		-\|Entity\|aSHM\|Significant selection\|dN/dS (missense)\|dN/dS (nonsense)\|
28		-\|:------:\|:----:\|:---------------------:\|:----------------:\|:----------------:\|
29		-\|BL \|No \|No \| 4.806 \|35.301 \|
30		-\|DLBCL \|No \|No \| 2.325 \|47.239 \|
31		-\|FL \|No \|No \|16.820 \| 0.000 \|
32		-
33		-
34		-
35		-View coding variants in ProteinPaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/SYNCRIP_protein.html) or [hg38](https://morinlab.github.io/LLMPP/GAMBL/SYNCRIP_protein_hg38.html)
36		-
37		-![](images/proteinpaint/SYNCRIP_NM_006372.svg)
38		-
39		-View all variants in GenomePaint [hg19](https://morinlab.github.io/LLMPP/GAMBL/SYNCRIP.html) or [hg38](https://morinlab.github.io/LLMPP/GAMBL/SYNCRIP_hg38.html)
40		-
41		-![](images/proteinpaint/SYNCRIP.svg)
42		-
43		-## SYNCRIP Expression
44		-![](images/gene_expression/SYNCRIP_by_pathology.svg)
45		-<!-- ORIGIN: paneaWholeGenomeLandscape2019 -->
46		-<!-- BL: paneaWholeGenomeLandscape2019 -->
47		-
48		-## References
49		-1. Panea R, Love C, Shingleton JR, Reddy A, Bailey J, Moormann A, Otieno J, Ong’echa J, Oduor C, Schroêder K, Masalu N, Chao N, Agajanian M, Major M, Fedoriw Y, Richards K, Rymkiewicz G, Miles R, Alobeid B, Bhagat G, Flowers C, Ondrejka S, Hsi E, Choi W, Au-Yeung R, Hartmann W, Lenz G, Meyerson H, Lin YY, Zhuang Y, Luftig M, Waldrop A, Dave T, Thakkar D, Sahay H, Li G, Palus B, Seshadri V, Kim S, Gascoyne R, Levy S, Mukhopadhyay M, Dunson D, Dave S. The whole genome landscape of Burkitt lymphoma subtypes. Blood. 2019;