chr13:28018505:C>A Detail (hg38) (FLT3)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr13:28,592,642-28,592,642 View the variant detail on this assembly version. |
hg38 | chr13:28,018,505-28,018,505 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_004119.2:c.2503G>T | NP_004110.2:p.Asp835Tyr |
Ensemble | ENST00000241453.12:c.2503G>T | ENST00000241453.12:p.Asp835Tyr |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
CIViC
Disease | Drug | EL | ET | ED | CS | VO | TR | Pubmed | Links |
---|---|---|---|---|---|---|---|---|---|
acute myeloid leukemia | Quizartinib,Ponatinib | D |
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Resistance | Somatic | 3 | 23430109 | Detail |
acute myeloid leukemia | SU5614 | D |
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Resistance | Somatic | 3 | 19318574 | Detail |
acute myeloid leukemia | Sorafenib,Quizartinib | B |
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Resistance | Somatic | 4 | 22504184 | Detail |
acute myeloid leukemia | Sorafenib | B |
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Resistance | Somatic | 4 | 22368270 | Detail |
acute myeloid leukemia | Midostaurin | B |
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Sensitivity/Response | Somatic | 3 | 20733134 | Detail |
acute myeloid leukemia | Sorafenib | D |
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Resistance | Somatic | 1 | 23969938 | Detail |
acute myeloid leukemia | B |
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Better Outcome | Somatic | 3 | 17965322 | Detail | |
acute myeloid leukemia | B |
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Positive | Somatic | 3 | 11290608 | Detail | |
acute myeloid leukemia | Sorafenib | B |
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Resistance | Somatic | 4 | 22368270 | Detail |
acute myeloid leukemia | Sorafenib | B |
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Resistance | Somatic | 4 | 18230792 | Detail |
acute myeloid leukemia | B |
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N/A | Somatic | 3 | 11290608 | Detail | |
acute myeloid leukemia | B |
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Poor Outcome | Somatic | 4 | 17940205 | Detail |
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.560 | Leukemia, Myelocytic, Acute | NA | CLINVAR | Detail | |
0.130 | Acute lymphocytic leukemia | NA | CLINVAR | Detail | |
0.560 | Leukemia, Myelocytic, Acute | Our FLT3-Aurora kinase inhibitor, CCT137690, successfully inhibited growth of FL... | BeFree | 22354205 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
An in-vitro saturation mutagenesis screen of 50 independently derived FLT3-ITD clones was performed ... | CIViC Evidence | Detail |
An in-vitro cell-based screening approach generated FLT3-ITD-expressing cell lines resistant to the ... | CIViC Evidence | Detail |
In an in-vitro study using an in vitro saturation mutagenesis assay, 4 residues with AC220 (quizarti... | CIViC Evidence | Detail |
13 patients with relapsed or chemo-refractory FLT3-ITD+ AML were treated with sorafenib (200-400 mg ... | CIViC Evidence | Detail |
In a phase 2 clinical study of 95 AML/high-risk MDS patients treated with either 50 or 100 mg midost... | CIViC Evidence | Detail |
Mouse Ba/F3 cells with FLT3 mutations were evaluated for sorafenib resistance. Cells with single FL... | CIViC Evidence | Detail |
Event-free survival was significantly improved in patients with both NPM1 and FLT3-TKD mutations com... | CIViC Evidence | Detail |
WBC counts were not significantly different in AML patients with FLT3 D835 mutations compared to wil... | CIViC Evidence | Detail |
Emergence of D835 mutation in AML patients with FLT3 tandem repeat is associated with sorafenib resi... | CIViC Evidence | Detail |
Sorafenib is effective in patients with FLT3 internal tandem repeat mutations, but not in patients w... | CIViC Evidence | Detail |
AML patients with D835 mutation of FLT3 did not have worse overall survival than patients with wild ... | CIViC Evidence | Detail |
In AML patients, FLT3-TKD mutation was associated with poorer disease free survival compared to pati... | CIViC Evidence | Detail |
NM_004119.3(FLT3):c.2503G>T (p.Asp835Tyr) AND Acute myeloid leukemia | ClinVar | Detail |
NM_004119.3(FLT3):c.2503G>T (p.Asp835Tyr) AND Acute lymphoid leukemia | ClinVar | Detail |
NA | DisGeNET | Detail |
NA | DisGeNET | Detail |
Our FLT3-Aurora kinase inhibitor, CCT137690, successfully inhibited growth of FLT3-ITD-D835Y cells i... | DisGeNET | Detail |
Overlapped Transcript Coordinates
Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
---|
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs121913488 dbSNP
- Genome
- hg38
- Position
- chr13:28,018,505-28,018,505
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- A
- Variant (CIViC) (CIViC Variant)
- TKD MUTATION
- Transcript 1 (CIViC Variant)
- ENST00000241453.7
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/56
- Summary (CIViC Variant)
- FLT3 tyrosine kinase domain mutations (FLT3-TKD) are much less common than FLT3-ITD (internal tandem duplication) mutations and may not confer the same prognostic impact. Although the majority of mutations are point mutations effecting D835 (most frequently D835Y), a small proportion involve an in-frame deletion of I836. These mutations are within the activation loop of the second tyrosine kinase domain of FLT3 and thought to result in constitutive activation of the receptor.
- Variant (CIViC) (CIViC Variant)
- D835
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/437
- Variant (CIViC) (CIViC Variant)
- D835H/Y
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/613
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