Annotation Detail
Information
- Associated Genes
- ALK
- Associated Variants
-
ALK p.Arg1275Gln (p.R1275Q)
(
ENST00000389048.8,
ENST00000618119.4,
ENST00000642122.1 )
ALK p.Arg1275Gln (p.R1275Q) ( ENST00000389048.8, ENST00000618119.4, ENST00000642122.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_004304.5(ALK):c.3824G>A (p.Arg1275Gln) AND not provided
- ClinVar Allele ID
- 33122
- ClinVar RefSeq Alternation Syntax
- NM_001353765.2:c.620G>A
- ClinVar RefSeq Alternation Syntax
- NM_004304.5:c.3824G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2020-10-23
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001268655
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs