Annotation Detail
Information
- Associated Genes
- NF1
- Associated Variants
-
NF1 p.Cys93Tyr (p.C93Y)
(
ENST00000696138.1,
ENST00000358273.9,
ENST00000691014.1,
ENST00000356175.7,
ENST00000431387.8,
ENST00000487476.5,
ENST00000490416.2 )
NF1 p.Cys93Tyr (p.C93Y) ( ENST00000356175.7, ENST00000358273.9, ENST00000431387.8, ENST00000487476.5, ENST00000490416.2, ENST00000691014.1, ENST00000696138.1 ) - Associated Disease
- juvenile myelomonocytic leukemia
- Source Database
- ClinVar
- Description
- NM_001042492.3(NF1):c.278G>A (p.Cys93Tyr) AND Juvenile myelomonocytic leukemia
- ClinVar Allele ID
- 79219
- ClinVar RefSeq Alternation Syntax
- NM_001042492.3:c.278G>A
- ClinVar RefSeq Alternation Syntax
- NM_001128147.3:c.278G>A
- ClinVar RefSeq Alternation Syntax
- NM_000267.3:c.278G>A
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2022-10-29
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003460652
- ClinVar Disease
- Juvenile myelomonocytic leukemia
- Observed Origin Sample
- unknown
Drugs