Annotation Detail
Information
- Associated Genes
- BRAF
- Associated Variants
-
BRAF p.Leu245Phe (p.L245F)
(
ENST00000288602.11,
ENST00000496384.7,
ENST00000644969.2,
ENST00000646891.2 )
BRAF p.Leu245Phe (p.L245F) ( ENST00000288602.11, ENST00000496384.7, ENST00000644969.2, ENST00000646891.2 ) - Associated Disease
- Noonan syndrome with multiple lentigines
- Source Database
- ClinVar
- Description
- NM_004333.6(BRAF):c.735A>T (p.Leu245Phe) AND Noonan syndrome with multiple lentigines
- ClinVar Allele ID
- 48818
- ClinVar RefSeq Alternation Syntax
- NM_001378472.1:c.579A>T
- ClinVar RefSeq Alternation Syntax
- NM_001378468.1:c.735A>T
- ClinVar RefSeq Alternation Syntax
- NM_004333.6:c.735A>T
- ClinVar RefSeq Alternation Syntax
- NM_001374258.1:c.735A>T
- ClinVar RefSeq Alternation Syntax
- NM_001378475.1:c.471A>T
- ClinVar RefSeq Alternation Syntax
- NM_001378474.1:c.735A>T
- ClinVar RefSeq Alternation Syntax
- NM_001378467.1:c.744A>T
- ClinVar RefSeq Alternation Syntax
- NM_001378469.1:c.735A>T
- ClinVar RefSeq Alternation Syntax
- NM_001378473.1:c.579A>T
- ClinVar RefSeq Alternation Syntax
- NM_001354609.2:c.735A>T
- ClinVar RefSeq Alternation Syntax
- NM_001378471.1:c.735A>T
- ClinVar RefSeq Alternation Syntax
- NM_001374244.1:c.735A>T
- ClinVar RefSeq Alternation Syntax
- NM_001378470.1:c.633A>T
- Clinical Significance Description
- not provided
- Clinical Significance Review Status
- no assertion provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000055897
- ClinVar Disease
- Noonan syndrome with multiple lentigines
- Observed Origin Sample
- unknown
Drugs