[Paper-level Aggregated] PMCID: PMC4741605

Evidence Type(s): Oncogenic

Summary: Mutation: D835Y | Summary: The D835Y mutation is associated with the presence of small TKD mutated clones in the patient, indicating its contribution to tumor development or progression. It is part of a clone that is monitored during disease progression, and its increase in frequency at relapse suggests a correlation with tumor behavior and disease outcome independent of therapy.

Evidence Type: Oncogenic Mutation: D839G | Summary: The D839G mutation is part of the small TKD mutated clones observed in the patient, suggesting its role in tumor development or progression.

Gene→Variant (gene-first): FLT3(2322):D835Y FLT3(2322):D839G

Genes: FLT3(2322)

Variants: D835Y D839G

[Paper-level Aggregated] PMCID: PMC4741605

Evidence Type(s): Prognostic

Summary: Mutation: D835Y | Summary: The increase in the D835Y mutated clone at relapse suggests that this mutation may correlate with disease outcome independent of therapy, highlighting its prognostic significance.

Gene→Variant (gene-first): FLT3(2322):D835Y

Genes: FLT3(2322)

Variants: D835Y

[Paper-level Aggregated] PMCID: PMC4741605

Evidence Type(s): Predictive

Summary: Mutation: D835H | Summary: The D835H mutation is associated with resistance to Sorafenib treatment, indicating its predictive value in therapy response.

Evidence Type: Predictive Mutation: D839G | Summary: The D839G mutation is linked to resistance to Sorafenib treatment, suggesting it has predictive implications for therapy response.

Evidence Type: Predictive Mutation: D835Y | Summary: The D835Y mutation is associated with the patient's response to chemotherapy treatment and was successfully inhibited by treatment, indicating its relevance in predicting treatment outcomes.

Gene→Variant (gene-first): FLT3(2322):D835H FLT3(2322):D839G FLT3(2322):D835Y

Genes: FLT3(2322)

Variants: D835H D839G D835Y

[Paragraph-level] PMCID: PMC4741605 Section: RESULTS PassageIndex: 20

Evidence Type(s): Predictive, Prognostic, Oncogenic

Summary: Evidence Type: Predictive | Mutation: D835Y | Summary: The D835Y mutation is associated with the patient's response to chemotherapy treatment, indicating its relevance in predicting treatment outcomes. Evidence Type: Prognostic | Mutation: D835Y | Summary: The increase in the D835Y mutated clone at relapse suggests that this mutation may correlate with disease outcome independent of therapy, highlighting its prognostic significance. Evidence Type: Oncogenic | Mutation: D835Y | Summary: The D835Y mutation contributes to tumor development or progression, as indicated by its increase in frequency at relapse.

Gene→Variant (gene-first): 2322:D835Y

Genes: 2322

Variants: D835Y

[Paragraph-level] PMCID: PMC4741605 Section: RESULTS PassageIndex: 19

Evidence Type(s): Predictive, Oncogenic

Summary: Evidence Type: Predictive | Mutation: D835Y | Summary: The D835Y mutation was successfully inhibited by treatment, indicating a correlation with treatment response. Evidence Type: Oncogenic | Mutation: D835Y | Summary: The presence of the D835Y mutation is associated with tumor behavior, as it is part of a clone that is monitored during disease progression.

Gene→Variant (gene-first): 2322:D835Y

Genes: 2322

Variants: D835Y

[Paragraph-level] PMCID: PMC4741605 Section: RESULTS PassageIndex: 18

Evidence Type(s): Predictive

Summary: Evidence Type: Predictive | Mutation: D835H | Summary: The D835H mutation is associated with resistance to Sorafenib treatment, indicating its predictive value in therapy response. Evidence Type: Predictive | Mutation: D839G | Summary: The D839G mutation is also linked to resistance to Sorafenib treatment, suggesting it has predictive implications for therapy response.

Gene→Variant (gene-first): 2322:D835H 2322:D839G

Genes: 2322

Variants: D835H D839G

[Paragraph-level] PMCID: PMC4741605 Section: RESULTS PassageIndex: 17

Evidence Type(s): Oncogenic

Summary: Evidence Type: Oncogenic | Mutation: D835Y | Summary: The D835Y mutation is associated with the presence of small TKD mutated clones in the patient, indicating its contribution to tumor development or progression. Evidence Type: Oncogenic | Mutation: D839G | Summary: The D839G mutation is also part of the small TKD mutated clones observed in the patient, suggesting its role in tumor development or progression.

Gene→Variant (gene-first): 2322:D835Y 2322:D839G

Genes: 2322

Variants: D835Y D839G

[Paper-level Aggregated] PMCID: PMC4741605

Evidence Type(s): Oncogenic, Prognostic, Predictive

Justification: Oncogenic: The presence of mutations D835Y, D839G, and D835H in FLT3 is associated with resistance to treatment and disease progression, indicating their role in oncogenesis. Prognostic: The mutations D835Y and D839G are linked to the patient's response to therapy and the likelihood of relapse, suggesting they can provide prognostic information regarding disease outcome. Predictive: The mutations D835Y, D839G, and D835H are associated with resistance to Sorafenib treatment, indicating their potential to predict treatment response.

Gene→Variant (gene-first): FLT3(2322):D835H FLT3(2322):D839G FLT3(2322):D835Y

Genes: FLT3(2322)

Variants: D835H D839G D835Y

[Paragraph-level] PMCID: PMC4741605 Section: RESULTS PassageIndex: 20

Evidence Type(s): Predictive, Oncogenic

Justification: Predictive: The passage discusses the response of the patient to chemotherapy treatment and how the presence of the D835Y mutation correlates with the patient's relapse, indicating its potential role in therapeutic decisions. Oncogenic: The D835Y mutation is described as a mutation that contributes to the tumor's behavior, particularly in the context of the patient's relapse and the increase in the mutated clone's percentage.

Gene→Variant (gene-first): 2322:D835Y

Genes: 2322

Variants: D835Y

[Paragraph-level] PMCID: PMC4741605 Section: RESULTS PassageIndex: 19

Evidence Type(s): Predictive, Oncogenic

Justification: Predictive: The passage discusses the resistance of the D835Y variant to conventional induction chemotherapy and indicates that the treatment successfully inhibited the D835Y mutated clone, suggesting a correlation with treatment response. Oncogenic: The D835Y variant is mentioned in the context of tumor progression and its behavior in response to treatment, indicating its role in tumor development or progression.

Gene→Variant (gene-first): 2322:D835Y

Genes: 2322

Variants: D835Y

[Paragraph-level] PMCID: PMC4741605 Section: RESULTS PassageIndex: 18

Evidence Type(s): Predictive, Oncogenic

Justification: Predictive: The passage states that the mutations D839G and D835H are able to confer resistance to Sorafenib treatment, indicating a correlation between these variants and treatment response. Oncogenic: The presence of the D839G and D835H mutations is associated with the evolution of the FLT3 ITD+ clone and suggests a role in tumor development or progression, particularly in the context of acute myeloid leukemia (AML).

Gene→Variant (gene-first): 2322:D835H 2322:D839G

Genes: 2322

Variants: D835H D839G

[Paragraph-level] PMCID: PMC4741605 Section: RESULTS PassageIndex: 17

Evidence Type(s): Predictive, Oncogenic

Justification: Predictive: The passage discusses the patient's response to the FLT3 inhibitor AC220-002, indicating that the presence of the D835Y and D839G variants may correlate with the patient's treatment response. Oncogenic: The D835Y and D839G variants are mentioned in the context of their abundance in the patient's sample, suggesting their potential role in tumor development or progression as part of the FLT3 mutation landscape.

Gene→Variant (gene-first): 2322:D835Y 2322:D839G

Genes: 2322

Variants: D835Y D839G

[Paragraph-level] PMCID: PMC4741605 Section: RESULTS PassageIndex: 20

Evidence Type(s): Predictive, Oncogenic

Justification: Predictive: The passage discusses the response of the patient to chemotherapy treatment and how the presence of the D835Y mutation correlates with the patient's relapse, indicating its potential role in therapeutic decisions. Oncogenic: The D835Y mutation is described as a mutation that contributes to the tumor's behavior, particularly in the context of the patient's relapse and the increase in the mutated clone's percentage.

Gene→Variant (gene-first): 2322:D835Y

Genes: 2322

Variants: D835Y

[Paragraph-level] PMCID: PMC4741605 Section: RESULTS PassageIndex: 19

Evidence Type(s): Predictive, Oncogenic

Justification: Predictive: The passage discusses the resistance of the D835Y variant to conventional induction chemotherapy and indicates that the treatment successfully inhibited the D835Y mutated clone, suggesting a correlation with treatment response. Oncogenic: The D835Y variant is mentioned in the context of tumor progression and its behavior in response to treatment, indicating its role in tumor development or progression.

Gene→Variant (gene-first): 2322:D835Y

Genes: 2322

Variants: D835Y

[Paragraph-level] PMCID: PMC4741605 Section: RESULTS PassageIndex: 18

Evidence Type(s): Predictive, Oncogenic

Justification: Predictive: The passage states that the mutations D839G and D835H are able to confer resistance to Sorafenib treatment, indicating a correlation between these variants and treatment response. Oncogenic: The presence of the D839G and D835H mutations is associated with the evolution of the FLT3 ITD+ clone and suggests a role in tumor development or progression, particularly in the context of acute myeloid leukemia (AML).

Gene→Variant (gene-first): 2322:D835H 2322:D839G

Genes: 2322

Variants: D835H D839G

[Paragraph-level] PMCID: PMC4741605 Section: RESULTS PassageIndex: 17

Evidence Type(s): Predictive, Oncogenic

Justification: Predictive: The passage discusses the patient's response to the FLT3 inhibitor AC220-002, indicating that the presence of the D835Y and D839G variants may correlate with the patient's treatment response. Oncogenic: The D835Y and D839G variants are mentioned in the context of their abundance in the patient's sample, suggesting their potential role in tumor development or progression as part of the FLT3 mutation landscape.

Gene→Variant (gene-first): 2322:D835Y 2322:D839G

Genes: 2322

Variants: D835Y D839G