Annotation Detail
Information
- Associated Genes
- BUB1B
- Associated Variants
-
BUB1B p.Leu844Phe (p.L844F)
(
ENST00000287598.11,
ENST00000412359.7 )
BUB1B p.Leu844Phe (p.L844F) ( ENST00000287598.11, ENST00000412359.7 ) - Associated Disease
- colorectal cancer Premature chromatid separation trait mosaic variegated aneuploidy syndrome 1
- Source Database
- ClinVar
- Description
- NM_001211.6(BUB1B):c.2530C>T (p.Leu844Phe) AND multiple conditions
- ClinVar Allele ID
- 21800
- ClinVar RefSeq Alternation Syntax
- NM_001211.6:c.2530C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2022-01-10
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002504759
- ClinVar Disease
- Colorectal cancer
- ClinVar Disease
- Mosaic variegated aneuploidy syndrome 1
- ClinVar Disease
- Premature chromatid separation trait
- Observed Origin Sample
- unknown
Drugs