Annotation Detail
Information
- Associated Genes
- EYS
- Associated Variants
-
EYS p.Asn2565MetfsTer52 (p.N2565Mfs*52)
(
ENST00000503581.6,
ENST00000370621.7 )
EYS p.Asn2565MetfsTer52 (p.N2565Mfs*52) ( ENST00000370621.7, ENST00000503581.6 ) - Associated Disease
- retinitis pigmentosa
- Source Database
- ClinVar
- Description
- NM_001142800.2(EYS):c.7694del (p.Asn2565fs) AND Retinitis pigmentosa
- ClinVar Allele ID
- 152828
- ClinVar RefSeq Alternation Syntax
- NM_001142800.2:c.7694del
- ClinVar RefSeq Alternation Syntax
- NM_001292009.2:c.7694del
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000132631
- ClinVar Disease
- Retinitis pigmentosa
- Observed Origin Sample
- not provided
Drugs