Annotation Detail
Information
- Associated Genes
- BRAF
- Associated Variants
-
BRAF p.Trp571Cys (p.W571C)
(
ENST00000288602.11,
ENST00000496384.7,
ENST00000644969.2,
ENST00000646891.2 )
BRAF p.Trp571Cys (p.W571C) ( ENST00000288602.11, ENST00000496384.7, ENST00000644969.2, ENST00000646891.2 ) - Associated Disease
- Noonan syndrome 7
- Source Database
- ClinVar
- Description
- NM_004333.6(BRAF):c.1593G>C (p.Trp531Cys) AND Noonan syndrome 7
- ClinVar Allele ID
- 38763
- ClinVar RefSeq Alternation Syntax
- NM_001374244.1:c.1713G>C
- ClinVar RefSeq Alternation Syntax
- NM_001378467.1:c.1602G>C
- ClinVar RefSeq Alternation Syntax
- NM_001374258.1:c.1713G>C
- ClinVar RefSeq Alternation Syntax
- NM_001378472.1:c.1437G>C
- ClinVar RefSeq Alternation Syntax
- NM_001378470.1:c.1491G>C
- ClinVar RefSeq Alternation Syntax
- NM_001378474.1:c.1593G>C
- ClinVar RefSeq Alternation Syntax
- NM_001378469.1:c.1527G>C
- ClinVar RefSeq Alternation Syntax
- NM_001378471.1:c.1482G>C
- ClinVar RefSeq Alternation Syntax
- NM_001354609.2:c.1593G>C
- ClinVar RefSeq Alternation Syntax
- NM_001378473.1:c.1437G>C
- ClinVar RefSeq Alternation Syntax
- NM_001378468.1:c.1593G>C
- ClinVar RefSeq Alternation Syntax
- NM_001378475.1:c.1329G>C
- ClinVar RefSeq Alternation Syntax
- NM_004333.6:c.1593G>C
- 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/RCV000022682
- ClinVar Disease
- Noonan syndrome 7
- Observed Origin Sample
- germline
- Pubmed
- 19206169
Drugs