Variant · Snv
FLT3 D835V
CI-VAR-00000578Explore in graph →NP_004110.2:p.Asp835ValNM_004119.2:c.2504A>TClinVar 16272 CIViC 1302 rs121909646
Curated evidence
Evidence by cancer (14 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
- Source
- CIViC — Clinical Interpretation of Variants in Cancer
- Dataset
- CIViC evidence items
- Version
- civic-2026-09-08
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- expert curation
- License
- CC0 1.0
- PMID
- 26297285
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Acute Myeloid Leukemia13 | ||||||||
| FLT3 D835V | (diagnostic) | Diagnostic | B | Supports Positive | 2 | submitted | EID3002The study is conducted with 144 AML patients. 6 of the normal karyotype patients with AML(n = 51), have FLT3 mutation. 2 of these mutations have been reported as D835V mutations.(%33 among FLT3 mutati… (full text at CIViC) PMID 26297285 · El Halabi et al., 2015 · Open in CIViC | civic |
| FLT3 D835V | (diagnostic) | Diagnostic | B | Supports Positive | 3 | submitted | EID3011429 AML, 29 MDS, 36 ALL, 14 adult T-Cell leukemia, 17 malignant lymphoma, 10 CLL, 40 multiple myeloma, 11 CML and 3 essential thrombocytosis patients were analyzed for FLT3 gen mutation and FLT3 D835… (full text at CIViC) PMID 11290608 · Yamamoto et al., 2001 · Open in CIViC | civic |
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 16272 | Pathogenic | no assertion criteria provided | 0 | Acute myeloid leukemia; Acute lymphoid leukemia | somatic | 1 | May 01, 2004 | clinvar |