Annotation Detail
Information
- Associated Genes
- NF1
- Associated Variants
-
NF1 p.Arg192Ter (p.R192*)
(
ENST00000490416.2,
ENST00000487476.5,
ENST00000356175.7,
ENST00000358273.9,
ENST00000431387.8,
ENST00000691014.1,
ENST00000696138.1 )
NF1 p.Arg192Ter (p.R192*) ( ENST00000356175.7, ENST00000358273.9, ENST00000431387.8, ENST00000487476.5, ENST00000490416.2, ENST00000691014.1, ENST00000696138.1 ) - Associated Disease
- Neurofibromatosis, type 1
- Source Database
- ClinVar
- Description
- NM_001042492.3(NF1):c.574C>T (p.Arg192Ter) AND Neurofibromatosis, type 1
- Observed Origin Sample
- unknown
- Pubmed
- 15846561
- Pubmed
- 17406642
- ClinVar Allele ID
- 48599
- ClinVar RefSeq Alternation Syntax
- NM_001128147.3:c.574C>T
- ClinVar RefSeq Alternation Syntax
- NM_000267.3:c.574C>T
- ClinVar RefSeq Alternation Syntax
- NM_001042492.3:c.574C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-12-31
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000033171
- ClinVar Disease
- Neurofibromatosis, type 1
- Observed Origin Sample
- germline
Drugs