Annotation Detail
Information
- Associated Genes
- ABCB4
- Associated Variants
-
ABCB4 p.Arg957Ter (p.R957*)
(
ENST00000265723.8,
ENST00000453593.5,
ENST00000359206.8,
ENST00000649586.2 )
ABCB4 p.Arg957Ter (p.R957*) ( ENST00000265723.8, ENST00000359206.8, ENST00000453593.5, ENST00000649586.2 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000443.4(ABCB4):c.2869C>T (p.Arg957Ter) AND not provided
- ClinVar Allele ID
- 28726
- ClinVar RefSeq Alternation Syntax
- NM_000443.4:c.2869C>T
- ClinVar RefSeq Alternation Syntax
- NM_018849.3:c.2869C>T
- ClinVar RefSeq Alternation Syntax
- NM_018850.3:c.2783+1669C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-06-25
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001781265
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs