Annotation Detail
Information
- Associated Genes
- OPA1
- Associated Variants
-
OPA1 p.Arg818Trp (p.R818W)
(
ENST00000361150.6,
ENST00000361510.8,
ENST00000361715.6,
ENST00000361828.7,
ENST00000361908.8,
ENST00000392436.7,
ENST00000392437.6,
ENST00000643329.1,
ENST00000645553.1,
ENST00000646793.1 )
OPA1 p.Arg818Trp (p.R818W) ( ENST00000361150.6, ENST00000361510.8, ENST00000361715.6, ENST00000361828.7, ENST00000361908.8, ENST00000392436.7, ENST00000392437.6, ENST00000643329.1, ENST00000645553.1, ENST00000646793.1 ) - Associated Disease
- Autosomal dominant optic atrophy classic form
- Source Database
- ClinVar
- Description
- NM_130837.3(OPA1):c.2506C>T (p.Arg836Trp) AND Autosomal dominant optic atrophy classic form
- ClinVar Allele ID
- 211003
- ClinVar RefSeq Alternation Syntax
- NM_001354664.2:c.1969C>T
- ClinVar RefSeq Alternation Syntax
- NM_130835.3:c.2398C>T
- ClinVar RefSeq Alternation Syntax
- NM_130836.3:c.2452C>T
- ClinVar RefSeq Alternation Syntax
- NM_130834.3:c.2395C>T
- ClinVar RefSeq Alternation Syntax
- NM_130837.3:c.2506C>T
- ClinVar RefSeq Alternation Syntax
- NM_130832.3:c.2287C>T
- ClinVar RefSeq Alternation Syntax
- NM_130833.3:c.2344C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354663.2:c.1972C>T
- ClinVar RefSeq Alternation Syntax
- NM_015560.3:c.2341C>T
- ClinVar RefSeq Alternation Syntax
- NM_130831.3:c.2233C>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2017-04-27
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000287680
- ClinVar Disease
- Autosomal dominant optic atrophy classic form
- Observed Origin Sample
- germline
Drugs