MET EXON 14 MUTATION + AMPLIFICATION Detail (hg38) (MET)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr7:116,312,459-116,436,396 View the variant detail on this assembly version. |
| hg38 | chr7:116,672,405-116,796,342 |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
ClinVar
| Clinical Significance | |
| Review star | [No Data.] |
| Show details | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
| Disease | Drug | EL | ET | ED | CS | VO | TR | Pubmed | Links |
|---|---|---|---|---|---|---|---|---|---|
| lung non-small cell carcinoma | Crizotinib | C |
Predictive
|
Supports
|
Sensitivity/Response | Somatic | 3 | 26729443 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| 64-year old female (non-smoker) was diagnosed with NSCLC. A c.3028 G->A mutation was identified in e... | 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
- MET
- Genome
- hg38
- Position
- chr7:116,672,405-116,796,342
- Variant Type
- cnv
- Variant (CIViC) (CIViC Variant)
- EXON 14 MUTATION + AMPLIFICATION
- Transcript 1 (CIViC Variant)
- ENST00000318493.6
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/464
Genome browser