Annotation Detail
Information
- Associated Genes
- BRAF
- Associated Variants
-
BRAF p.Thr241Pro (p.T241P)
(
ENST00000288602.11,
ENST00000496384.7,
ENST00000644969.2,
ENST00000646891.2 )
BRAF p.Thr241Pro (p.T241P) ( ENST00000288602.11, ENST00000496384.7, ENST00000644969.2, ENST00000646891.2 ) - Associated Disease
- cardiofaciocutaneous syndrome 1 LEOPARD syndrome 3 lung carcinoma Noonan syndrome 7 Noonan syndrome 1
- Source Database
- ClinVar
- Description
- NM_004333.6(BRAF):c.721A>C (p.Thr241Pro) AND multiple conditions
- ClinVar Allele ID
- 38762
- ClinVar RefSeq Alternation Syntax
- NM_001378472.1:c.565A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378468.1:c.721A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378470.1:c.619A>C
- ClinVar RefSeq Alternation Syntax
- NM_004333.6:c.721A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378467.1:c.730A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378475.1:c.457A>C
- ClinVar RefSeq Alternation Syntax
- NM_001374258.1:c.721A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378469.1:c.721A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378473.1:c.565A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378474.1:c.721A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378471.1:c.721A>C
- ClinVar RefSeq Alternation Syntax
- NM_001354609.2:c.721A>C
- ClinVar RefSeq Alternation Syntax
- NM_001374244.1:c.721A>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2017-05-18
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000515363
- ClinVar Disease
- LEOPARD syndrome 3
- ClinVar Disease
- Cardiofaciocutaneous syndrome 1
- ClinVar Disease
- Noonan syndrome 7
- ClinVar Disease
- Lung carcinoma
- ClinVar Disease
- Noonan syndrome 1
- Observed Origin Sample
- unknown
Drugs