KIT AMPLIFICATION Detail (hg19) (KIT)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr4:55,524,085-55,606,881 |
hg38 | chr4:54,657,918-54,740,715 View the variant detail on this assembly version. |
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 |
---|---|---|---|---|---|---|---|---|---|
mucosal melanoma | Imatinib | B |
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Resistance |
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3 | 23775962 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Phase 2 trial in metastatic mucosal, acral or chronically sun-damaged melanoma. Twenty-five patients... | 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
- KIT
- Genome
- hg19
- Position
- chr4:55,524,085-55,606,881
- Variant Type
- cnv
- Variant (CIViC) (CIViC Variant)
- AMPLIFICATION
- Transcript 1 (CIViC Variant)
- ENST00000288135.5
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/586
Genome browser