Annotation Detail
Information
- Associated Genes
- ALK
- Associated Variants
-
ALK p.Thr1151Met (p.T1151M)
(
ENST00000389048.8,
ENST00000618119.4,
ENST00000642122.1 )
ALK p.Thr1151Met (p.T1151M) ( ENST00000389048.8, ENST00000618119.4, ENST00000642122.1 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_004304.5(ALK):c.3452C>T (p.Thr1151Met) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 33125
- ClinVar RefSeq Alternation Syntax
- NM_001353765.2:c.248C>T
- ClinVar RefSeq Alternation Syntax
- NM_004304.5:c.3452C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2022-02-28
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001020341
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs