Annotation Detail
Information
- Associated Genes
- NF1
- Associated Variants
-
NF1 p.Asn974Ser (p.N974S)
(
ENST00000358273.9,
ENST00000356175.7,
ENST00000691014.1,
ENST00000696138.1 )
NF1 p.Asn974Ser (p.N974S) ( ENST00000696138.1, ENST00000356175.7, ENST00000358273.9, ENST00000691014.1 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_001042492.3(NF1):c.2921A>G (p.Asn974Ser) AND Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
- ClinVar Allele ID
- 184612
- ClinVar RefSeq Alternation Syntax
- NM_000267.3:c.2921A>G
- ClinVar RefSeq Alternation Syntax
- NM_001042492.3:c.2921A>G
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2021-09-18
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000165243
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
Drugs