GRCh38/hg38 9p21.3(chr9:21939409-22706614)x0 Detail (hg19) (CDKN2A, CDKN2B, MTAP, CDKN2A-AS1, DMRTA1, LINC01239, CDKN2B-AS1, LOC114022702, LOC126860595, LOC126860596, LOC126860597, LOC128772337, LOC128772338, LOC128772339, LOC130001602, LOC130001603, LOC130001604, LOC130001605, LOC130001606, LOC130001607, LOC130001608, LOC130001609, LOC130001610)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr9:21,939,408-22,706,613 |
| hg38 | chr9:21,939,409-22,706,614 View the variant detail on this assembly version. |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
ClinVar
| Clinical Significance |
drug response
|
| Review star |  |
| Show details | |
Links
| Type | Database | ID | Link |
|---|---|---|---|
| Gene | MIM | ||
| HGNC | |||
| Ensembl | |||
| NCBI | |||
| Gene Cards | |||
| OncoKB |
| Type | Database | ID | Link |
|---|---|---|---|
| Variant | TogoVar | ||
| COSMIC | |||
| MONDO |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
|
drug response
|
2017-11-27 | no assertion criteria provided |
somatic
|
Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| GRCh38/hg38 9p21.3(chr9:21939409-22706614)x0 AND Vascular endothelial growth factor (VEGF) inhibitor... | ClinVar | 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
- chr9:21,939,408-22,706,613
- Variant Type
- cnv
Genome browser