Annotation Detail
Information
- Associated Genes
- RAF1
- Associated Variants
-
RAF1 p.Pro261Thr (p.P261T)
(
ENST00000251849.9,
ENST00000442415.7,
ENST00000685437.1,
ENST00000685653.1,
ENST00000687923.1,
ENST00000688543.1,
ENST00000689389.1,
ENST00000690397.1,
ENST00000690460.1,
ENST00000691899.1,
ENST00000692093.1,
ENST00000693312.1 )
RAF1 p.Pro261Thr (p.P261T) ( ENST00000251849.9, ENST00000442415.7, ENST00000685437.1, ENST00000685653.1, ENST00000687923.1, ENST00000688543.1, ENST00000689389.1, ENST00000690397.1, ENST00000690460.1, ENST00000691899.1, ENST00000692093.1, ENST00000693312.1 ) - Associated Disease
- Noonan syndrome
- Source Database
- ClinVar
- Description
- NM_002880.4(RAF1):c.781C>A (p.Pro261Thr) AND Noonan syndrome
- ClinVar Allele ID
- 49074
- ClinVar RefSeq Alternation Syntax
- NM_001354689.3:c.781C>A
- ClinVar RefSeq Alternation Syntax
- NM_001354695.3:c.439C>A
- ClinVar RefSeq Alternation Syntax
- NM_001354694.3:c.538C>A
- ClinVar RefSeq Alternation Syntax
- NM_001354693.3:c.682C>A
- ClinVar RefSeq Alternation Syntax
- NM_001354692.3:c.538C>A
- ClinVar RefSeq Alternation Syntax
- NM_001354691.3:c.538C>A
- ClinVar RefSeq Alternation Syntax
- NR_148940.3:n.1112C>A
- ClinVar RefSeq Alternation Syntax
- NR_148942.3:n.1112C>A
- ClinVar RefSeq Alternation Syntax
- NM_002880.4:c.781C>A
- ClinVar RefSeq Alternation Syntax
- NM_001354690.3:c.781C>A
- ClinVar RefSeq Alternation Syntax
- NR_148941.3:n.1112C>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2011-04-15
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000037703
- ClinVar Disease
- Noonan syndrome
- Observed Origin Sample
- germline
Drugs