chr7:55181335:> Detail (hg38) (EGFR)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr7:55,249,028-55,249,030 |
| hg38 | chr7:55,181,335-55,181,337 |
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 |
|---|---|---|---|---|---|---|---|---|---|
| lung non-small cell carcinoma | Erlotinib | D |
Predictive
|
Supports
|
Sensitivity/Response | Somatic | 19147750 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| In an in vitro study, a Ba/F3 cell line expressing EGFR R776C demonstrated increased sensitivity to ... | 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
- hg38
- Position
- chr7:55,181,335-55,181,337
- Variant Type
- snv
- Variant (CIViC) (CIViC Variant)
- R776C
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/1181
Genome browser