Annotation Detail
Information
- Associated Genes
- BRAF
- Associated Variants
-
BRAF p.Phe635Leu (p.F635L)
(
ENST00000288602.11,
ENST00000496384.7,
ENST00000644969.2,
ENST00000646891.2 )
BRAF p.Phe635Leu (p.F635L) ( ENST00000288602.11, ENST00000496384.7, ENST00000644969.2, ENST00000646891.2 ) - Associated Disease
- RASopathy
- Source Database
- ClinVar
- Description
- NM_004333.6(BRAF):c.1785T>G (p.Phe595Leu) AND RASopathy
- ClinVar Allele ID
- 174042
- ClinVar RefSeq Alternation Syntax
- NM_001378469.1:c.1719T>G
- ClinVar RefSeq Alternation Syntax
- NM_001378471.1:c.1674T>G
- ClinVar RefSeq Alternation Syntax
- NM_001378467.1:c.1794T>G
- ClinVar RefSeq Alternation Syntax
- NM_001354609.2:c.1785T>G
- ClinVar RefSeq Alternation Syntax
- NM_001378470.1:c.1683T>G
- ClinVar RefSeq Alternation Syntax
- NM_001374244.1:c.1905T>G
- ClinVar RefSeq Alternation Syntax
- NM_001378475.1:c.1521T>G
- ClinVar RefSeq Alternation Syntax
- NM_001378468.1:c.1785T>G
- ClinVar RefSeq Alternation Syntax
- NM_001378474.1:c.1785T>G
- ClinVar RefSeq Alternation Syntax
- NM_004333.6:c.1785T>G
- ClinVar RefSeq Alternation Syntax
- NM_001374258.1:c.1905T>G
- ClinVar RefSeq Alternation Syntax
- NM_001378472.1:c.1629T>G
- ClinVar RefSeq Alternation Syntax
- NM_001378473.1:c.1629T>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2017-04-03
- Clinical Significance Review Status
- reviewed by expert panel
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000522002
- ClinVar Disease
- RASopathy
- Observed Origin Sample
- germline
- Observed Origin Sample
- de novo
- Observed Origin Sample
- unknown
Drugs