Annotation Detail
Information
- Associated Genes
- ERCC2
- Associated Variants
-
ERCC2 p.Ala725Pro (p.A725P)
(
ENST00000391944.8,
ENST00000391945.10,
ENST00000684407.1 )
ERCC2 p.Ala725Pro (p.A725P) ( ENST00000391944.8, ENST00000391945.10, ENST00000684407.1 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_000400.4(ERCC2):c.2173G>C (p.Ala725Pro) AND Inborn genetic diseases
- ClinVar Allele ID
- 31820
- ClinVar RefSeq Alternation Syntax
- NM_000400.4:c.2173G>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-06-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003343601
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs