Annotation Detail
Information
- Associated Genes
- BRAF
- Associated Variants
-
BRAF p.Gly509Ter (p.G509*)
(
ENST00000288602.11,
ENST00000496384.7,
ENST00000644969.2,
ENST00000646891.2 )
BRAF p.Gly509Ter (p.G509*) ( ENST00000288602.11, ENST00000496384.7, ENST00000644969.2, ENST00000646891.2 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_004333.6(BRAF):c.1405G>T (p.Gly469Ter) AND not specified
- ClinVar Allele ID
- 174044
- ClinVar RefSeq Alternation Syntax
- NM_001378474.1:c.1405G>T
- ClinVar RefSeq Alternation Syntax
- NM_001378471.1:c.1294G>T
- ClinVar RefSeq Alternation Syntax
- NM_004333.6:c.1405G>T
- ClinVar RefSeq Alternation Syntax
- NM_001378469.1:c.1339G>T
- ClinVar RefSeq Alternation Syntax
- NM_001378472.1:c.1249G>T
- ClinVar RefSeq Alternation Syntax
- NM_001378473.1:c.1249G>T
- ClinVar RefSeq Alternation Syntax
- NM_001374258.1:c.1525G>T
- ClinVar RefSeq Alternation Syntax
- NM_001378475.1:c.1141G>T
- ClinVar RefSeq Alternation Syntax
- NM_001354609.2:c.1405G>T
- ClinVar RefSeq Alternation Syntax
- NM_001378468.1:c.1405G>T
- ClinVar RefSeq Alternation Syntax
- NM_001374244.1:c.1525G>T
- ClinVar RefSeq Alternation Syntax
- NM_001378467.1:c.1414G>T
- ClinVar RefSeq Alternation Syntax
- NM_001378470.1:c.1303G>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2013-05-03
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000150211
- ClinVar Disease
- not specified
- Observed Origin Sample
- somatic
Drugs