Annotation Detail
Information
- Associated Genes
- BUB1B BUB1B-PAK6
- Associated Variants
-
BUB1B p.Glu967Asp (p.E967D)
(
ENST00000412359.7,
ENST00000441369.6,
ENST00000287598.11,
ENST00000453867.7,
ENST00000558658.6 )
BUB1B p.Glu967Asp (p.E967D) ( ENST00000287598.11, ENST00000412359.7, ENST00000441369.6, ENST00000453867.7, ENST00000558658.6 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_001211.6(BUB1B):c.2901A>T (p.Glu967Asp) AND Inborn genetic diseases
- ClinVar Allele ID
- 643153
- ClinVar RefSeq Alternation Syntax
- NM_001128629.3:c.-118+839A>T
- ClinVar RefSeq Alternation Syntax
- NM_001211.6:c.2901A>T
- ClinVar RefSeq Alternation Syntax
- NM_001128628.3:c.-201+839A>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2021-09-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002433989
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs