Annotation Detail
Information
- Associated Genes
- BRAF
- Associated Variants
-
BRAF p.Lys641Gln (p.K641Q)
(
ENST00000288602.11,
ENST00000496384.7,
ENST00000644969.2,
ENST00000646891.2 )
BRAF p.Lys641Gln (p.K641Q) ( ENST00000288602.11, ENST00000496384.7, ENST00000644969.2, ENST00000646891.2 ) - Associated Disease
- Noonan syndrome Cardio-facio-cutaneous syndrome
- Source Database
- ClinVar
- Description
- NM_004333.6(BRAF):c.1801A>C (p.Lys601Gln) AND multiple conditions
- ClinVar Allele ID
- 49884
- ClinVar RefSeq Alternation Syntax
- NM_001374258.1:c.1921A>C
- ClinVar RefSeq Alternation Syntax
- NM_001354609.2:c.1801A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378469.1:c.1735A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378473.1:c.1645A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378471.1:c.1690A>C
- ClinVar RefSeq Alternation Syntax
- NM_004333.6:c.1801A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378468.1:c.1801A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378475.1:c.1537A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378470.1:c.1699A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378472.1:c.1645A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378474.1:c.1801A>C
- ClinVar RefSeq Alternation Syntax
- NM_001374244.1:c.1921A>C
- ClinVar RefSeq Alternation Syntax
- NM_001378467.1:c.1810A>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2019-01-02
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000150201
- ClinVar Disease
- Noonan syndrome
- ClinVar Disease
- Cardio-facio-cutaneous syndrome
- Observed Origin Sample
- germline
Drugs