Annotation Detail
Information
- Associated Genes
- EGFR
- Associated Variants
-
EGFR p.Asp761Tyr (p.D761Y)
(
ENST00000275493.7,
ENST00000450046.2,
ENST00000455089.5 )
EGFR p.Asp761Tyr (p.D761Y) ( ENST00000275493.7, ENST00000450046.2, ENST00000455089.5 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_005228.5(EGFR):c.2281G>T (p.Asp761Tyr) AND not specified
- ClinVar Allele ID
- 54411
- ClinVar RefSeq Alternation Syntax
- NM_001346899.2:c.2146G>T
- ClinVar RefSeq Alternation Syntax
- NM_001346898.2:c.2281G>T
- ClinVar RefSeq Alternation Syntax
- NM_005228.5:c.2281G>T
- ClinVar RefSeq Alternation Syntax
- NM_001346900.2:c.2122G>T
- ClinVar RefSeq Alternation Syntax
- NM_001346941.2:c.1480G>T
- ClinVar RefSeq Alternation Syntax
- NM_001346897.2:c.2146G>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2008-12-10
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000038400
- ClinVar Disease
- not specified
- Observed Origin Sample
- somatic
Drugs