Annotation Detail
Information
- Associated Genes
- EYS
- Associated Variants
-
EYS p.Phe1735GlnfsTer6 (p.F1735Qfs*6)
(
ENST00000503581.6,
ENST00000370621.7 )
EYS p.Phe1735GlnfsTer6 (p.F1735Qfs*6) ( ENST00000370621.7, ENST00000503581.6 ) - Associated Disease
- retinitis pigmentosa
- Source Database
- ClinVar
- Description
- NM_001142800.2(EYS):c.5202_5203del (p.Phe1735fs) AND Retinitis pigmentosa
- ClinVar Allele ID
- 152825
- ClinVar RefSeq Alternation Syntax
- NM_001292009.2:c.5202_5203del
- ClinVar RefSeq Alternation Syntax
- NM_001142800.2:c.5202_5203del
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000132628
- ClinVar Disease
- Retinitis pigmentosa
- Observed Origin Sample
- not provided
Drugs