Annotation Detail
Information
- Associated Genes
- EGFR
- Associated Variants
-
EGFR p.Leu858Arg (p.L858R)
(
ENST00000275493.7,
ENST00000450046.2,
ENST00000455089.5 )
EGFR p.Leu858Arg (p.L858R) ( ENST00000275493.7, ENST00000450046.2, ENST00000455089.5 ) - Associated Disease
- Nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, somatic
- Source Database
- ClinVar
- Description
- NM_005228.5(EGFR):c.2573T>G (p.Leu858Arg) AND Nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, somatic
- ClinVar Allele ID
- 31648
- ClinVar RefSeq Alternation Syntax
- NM_001346899.2:c.2438T>G
- ClinVar RefSeq Alternation Syntax
- NM_001346941.2:c.1772T>G
- ClinVar RefSeq Alternation Syntax
- NM_001346898.2:c.2573T>G
- ClinVar RefSeq Alternation Syntax
- NM_001346900.2:c.2414T>G
- ClinVar RefSeq Alternation Syntax
- NM_001346897.2:c.2438T>G
- ClinVar RefSeq Alternation Syntax
- NM_005228.5:c.2573T>G
- Clinical Significance Description
- drug response
- Clinical Significance Last Update
- 2005-05-19
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000018083
- ClinVar Disease
- Nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, somatic
- Observed Origin Sample
- somatic
- Pubmed
- 15118073
- Pubmed
- 15329413
- Pubmed
- 15118125
- Pubmed
- 15901872
Drugs