Annotation Detail
Information
- Associated Genes
- NF1
- Associated Variants
-
NF1 c.7189+3A>C
(
ENST00000691014.1,
ENST00000356175.7,
ENST00000687027.1,
ENST00000693617.1,
ENST00000358273.9,
ENST00000696138.1,
ENST00000684826.1 )
NF1 c.7189+3A>C ( ENST00000356175.7, ENST00000358273.9, ENST00000684826.1, ENST00000687027.1, ENST00000691014.1, ENST00000693617.1, ENST00000696138.1 ) - Associated Disease
- Neurofibromatosis, familial spinal
- Source Database
- ClinVar
- Description
- NM_001042492.3(NF1):c.7189+3A>C AND Neurofibromatosis, familial spinal
- ClinVar Allele ID
- 15408
- ClinVar RefSeq Alternation Syntax
- NM_001042492.3:c.7189+3A>C
- ClinVar RefSeq Alternation Syntax
- NM_000267.3:c.7126+3A>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2000-01-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000000400
- ClinVar Disease
- Neurofibromatosis, familial spinal
- Observed Origin Sample
- germline
- Pubmed
- 10862084
- Pubmed
- 1745350
Drugs