Annotation Detail
Information
- Associated Genes
- ALK
- Associated Variants
-
ALK p.Phe1174Val (p.F1174V)
(
ENST00000389048.8,
ENST00000618119.4,
ENST00000642122.1 )
ALK p.Phe1174Val (p.F1174V) ( ENST00000389048.8, ENST00000618119.4, ENST00000642122.1 ) - Associated Disease
- Neuroblastoma, susceptibility to, 3
- Source Database
- ClinVar
- Description
- NM_004304.5(ALK):c.3520T>G (p.Phe1174Val) AND Neuroblastoma, susceptibility to, 3
- ClinVar Allele ID
- 76578
- ClinVar RefSeq Alternation Syntax
- NM_001353765.2:c.316T>G
- ClinVar RefSeq Alternation Syntax
- NM_004304.5:c.3520T>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2015-10-07
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000055894
- ClinVar Disease
- Neuroblastoma, susceptibility to, 3
- Observed Origin Sample
- germline
- Observed Origin Sample
- somatic
Drugs