Annotation Detail
Information
- Associated Genes
- RAF1
- Associated Variants
-
RAF1 p.Pro261Arg (p.P261R)
(
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.Pro261Arg (p.P261R) ( 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.782C>G (p.Pro261Arg) AND Noonan syndrome
- ClinVar Allele ID
- 49076
- ClinVar RefSeq Alternation Syntax
- NR_148940.3:n.1113C>G
- ClinVar RefSeq Alternation Syntax
- NR_148941.3:n.1113C>G
- ClinVar RefSeq Alternation Syntax
- NR_148942.3:n.1113C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354689.3:c.782C>G
- ClinVar RefSeq Alternation Syntax
- NM_002880.4:c.782C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354692.3:c.539C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354693.3:c.683C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354690.3:c.782C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354691.3:c.539C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354695.3:c.440C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354694.3:c.539C>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2016-02-17
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000037706
- ClinVar Disease
- Noonan syndrome
- Observed Origin Sample
- germline
Drugs