Annotation Detail
Information
- Associated Genes
- ABCB1
- Associated Variants
-
ABCB1 p.Ser893Ala (p.S893A)
(
ENST00000265724.8,
ENST00000543898.5,
ENST00000622132.5 )
ABCB1 p.Ser893Ala (p.S893A) ( ENST00000265724.8, ENST00000543898.5, ENST00000622132.5 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_001348946.2(ABCB1):c.2677T>G (p.Ser893Ala) AND not specified
- ClinVar Allele ID
- 176988
- ClinVar RefSeq Alternation Syntax
- NM_001348944.2:c.2677T>G
- ClinVar RefSeq Alternation Syntax
- NM_001348945.2:c.2887T>G
- ClinVar RefSeq Alternation Syntax
- NM_000927.5:c.2677T>G
- ClinVar RefSeq Alternation Syntax
- NM_001348946.2:c.2677T>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2014-01-27
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000152717
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs