Annotation Detail
Information
- Associated Genes
- COL6A1
- Associated Variants
-
COL6A1 p.Tyr659= (p.Y659=)
(
ENST00000361866.8 )
COL6A1 p.Tyr659= (p.Y659=) ( ENST00000361866.8 ) - Associated Disease
- COL6A1-related disorder
- Source Database
- ClinVar
- Description
- NM_001848.3(COL6A1):c.1977C>T (p.Tyr659=) AND COL6A1-related disorder
- ClinVar Allele ID
- 757887
- ClinVar RefSeq Alternation Syntax
- NM_001848.3:c.1977C>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2019-06-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004533534
- ClinVar Disease
- COL6A1-related disorder
- Observed Origin Sample
- germline
Drugs