Annotation Detail
Information
- Associated Genes
- ACVRL1
- Associated Variants
-
ACVRL1 p.Ala482Val (p.A482V)
(
ENST00000388922.9,
ENST00000550683.5,
ENST00000419526.6,
ENST00000551576.6,
ENST00000547400.6,
ENST00000713619.1 )
ACVRL1 p.Ala482Val (p.A482V) ( ENST00000388922.9, ENST00000419526.6, ENST00000547400.6, ENST00000550683.5, ENST00000551576.6, ENST00000713619.1 ) - Source Database
- ClinVar
- Description
- NM_000020.3(ACVRL1):c.1445C>T (p.Ala482Val) AND multiple conditions
- ClinVar Allele ID
- 171155
- ClinVar RefSeq Alternation Syntax
- NM_000020.3:c.1445C>T
- ClinVar RefSeq Alternation Syntax
- NM_001077401.2:c.1445C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2020-05-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001270508
- Observed Origin Sample
- germline
Drugs