Annotation Detail
Information
- Associated Genes
- COL1A1
- Associated Variants
-
COL1A1 p.Gly1022Ser (p.G1022S)
(
ENST00000225964.10 )
COL1A1 p.Gly1022Ser (p.G1022S) ( ENST00000225964.10 ) - Associated Disease
- Osteogenesis imperfecta type III
- Source Database
- ClinVar
- Description
- NM_000088.4(COL1A1):c.3064G>A (p.Gly1022Ser) AND Osteogenesis imperfecta type III
- ClinVar Allele ID
- 32335
- ClinVar RefSeq Alternation Syntax
- NM_000088.4:c.3064G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 1989-11-25
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000018837
- ClinVar Disease
- Osteogenesis imperfecta type III
- Observed Origin Sample
- germline
- Pubmed
- 2511192
Drugs