chr17:37856333:> Detail (hg19) (ERBB2)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr17:37,856,333-37,884,915 |
| hg38 | chr17:39,700,080-39,728,662 |
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 |
|---|---|---|---|---|---|---|---|---|---|
| breast cancer | Lapatinib | B |
Predictive
|
Supports
|
Sensitivity/Response |
N/A
|
4 | 26811533 | Detail |
| breast cancer | B |
Prognostic
|
Supports
|
Poor Outcome |
N/A
|
3 | 26811533 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| Serum and tissue levels of HER2 (ERBB2) were analyzed in 1,902 breast cancer patients treated with l... | CIViC Evidence | Detail |
| Serum and tissue levels of HER2 (ERBB2) were analyzed in 1,902 breast cancer patients treated with l... | 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
- chr17:37,856,333-37,884,915
- Variant Type
- snv
- Variant (CIViC) (CIViC Variant)
- SERUM LEVELS
- Transcript 1 (CIViC Variant)
- ENST00000269571.5
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/416
Genome browser