ASNS AMPLIFICATION Detail (hg19) (ASNS)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr7:97,481,430-97,501,854 |
hg38 | chr7:97,852,118-97,872,542 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 |
---|---|---|---|---|---|---|---|---|---|
ovarian cancer | Asparaginase | D |
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Resistance | Somatic | 2 | 17088436 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
ASNS amplification and expression was associated with resistance to L-asparaginase in ovarian cancer... | 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
- ASNS
- Genome
- hg19
- Position
- chr7:97,481,430-97,501,854
- Variant Type
- cnv
- Variant (CIViC) (CIViC Variant)
- AMPLIFICATION
- Transcript 1 (CIViC Variant)
- ENST00000175506.4
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/409
Genome browser