Annotation Detail
Information
- Associated Genes
- BRAF
- Associated Variants
-
BRAF p.Glu541Ala (p.E541A)
(
ENST00000288602.11,
ENST00000496384.7,
ENST00000644969.2,
ENST00000646891.2 )
BRAF p.Glu541Ala (p.E541A) ( ENST00000288602.11, ENST00000496384.7, ENST00000644969.2, ENST00000646891.2 ) - Associated Disease
- Noonan syndrome
- Source Database
- ClinVar
- Description
- NM_004333.6(BRAF):c.1502A>C (p.Glu501Ala) AND Noonan syndrome
- ClinVar Allele ID
- 48843
- ClinVar RefSeq Alternation Syntax
- NM_001354609.2:c.1502A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378475.1:c.1238A>C
- ClinVar RefSeq Alternation Syntax
- NM_001374258.1:c.1622A>C
- ClinVar RefSeq Alternation Syntax
- NM_004333.6:c.1502A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378469.1:c.1436A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378473.1:c.1346A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378468.1:c.1502A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378472.1:c.1346A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378471.1:c.1391A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378470.1:c.1400A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378474.1:c.1502A>C
- ClinVar RefSeq Alternation Syntax
- NM_001374244.1:c.1622A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378467.1:c.1511A>C
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001261045
- ClinVar Disease
- Noonan syndrome
- Observed Origin Sample
- unknown
Drugs