Annotation Detail
Information
- Associated Genes
- BRAF
- Associated Variants
-
BRAF p.Thr241Arg (p.T241R)
(
ENST00000288602.11,
ENST00000496384.7,
ENST00000644969.2,
ENST00000646891.2 )
BRAF p.Thr241Arg (p.T241R) ( ENST00000288602.11, ENST00000496384.7, ENST00000644969.2, ENST00000646891.2 ) - Associated Disease
- Noonan syndrome 7
- Source Database
- ClinVar
- Description
- NM_004333.6(BRAF):c.722C>G (p.Thr241Arg) AND Noonan syndrome 7
- ClinVar Allele ID
- 38761
- ClinVar RefSeq Alternation Syntax
- NM_001374244.1:c.722C>G
- ClinVar RefSeq Alternation Syntax
- NM_001378470.1:c.620C>G
- ClinVar RefSeq Alternation Syntax
- NM_001374258.1:c.722C>G
- ClinVar RefSeq Alternation Syntax
- NM_001378469.1:c.722C>G
- ClinVar RefSeq Alternation Syntax
- NM_001378472.1:c.566C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354609.2:c.722C>G
- ClinVar RefSeq Alternation Syntax
- NM_001378471.1:c.722C>G
- ClinVar RefSeq Alternation Syntax
- NM_001378468.1:c.722C>G
- ClinVar RefSeq Alternation Syntax
- NM_004333.6:c.722C>G
- ClinVar RefSeq Alternation Syntax
- NM_001378467.1:c.731C>G
- ClinVar RefSeq Alternation Syntax
- NM_001378474.1:c.722C>G
- ClinVar RefSeq Alternation Syntax
- NM_001378475.1:c.458C>G
- ClinVar RefSeq Alternation Syntax
- NM_001378473.1:c.566C>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2009-04-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000022679
- ClinVar Disease
- Noonan syndrome 7
- Observed Origin Sample
- germline
- Pubmed
- 19206169
Drugs