chr10:123239371:> Detail (hg19) (FGFR2)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr10:123,239,371-123,357,917 |
hg38 | chr10:121,479,857-121,598,403 |
HGVS
Type | Transcript | Protein |
---|---|---|
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
[No Data.]
ClinVar
Clinical Significance | |
Review star | [No Data.] |
Show details |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
Disease | Drug | EL | ET | ED | CS | VO | TR | Pubmed | Links |
---|---|---|---|---|---|---|---|---|---|
endometrial cancer | Ponatinib | D |
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Sensitivity/Response | Somatic | 3 | 26574622 | Detail |
cholangiocarcinoma | Infigratinib | C |
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Sensitivity/Response | Somatic | 2 | 27870574 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Preclinical study in endometrial cancer cell lines (MFE-296, AN3CA, MFE-280 and Ishikawa). In cell p... | CIViC Evidence | Detail |
Phase 1 study of FGFR-inhibitor BGJ398 in advanced cancer with FGFR-aberrations. Among three patient... | CIViC Evidence | 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
- -
- Genome
- hg19
- Position
- chr10:123,239,371-123,357,917
- Variant Type
- snv
- Variant (CIViC) (CIViC Variant)
- MUTATION
- Transcript 1 (CIViC Variant)
- ENST00000457416.2
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/511
Genome browser