Annotation Detail
Information
- Associated Genes
- ERCC2
- Associated Variants
-
ERCC2 p.Leu461Val (p.L461V)
(
ENST00000391944.8,
ENST00000391945.10,
ENST00000684407.1 )
ERCC2 p.Leu461Val (p.L461V) ( ENST00000391944.8, ENST00000391945.10, ENST00000684407.1 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_000400.4(ERCC2):c.1381C>G (p.Leu461Val) AND Inborn genetic diseases
- ClinVar Allele ID
- 31818
- ClinVar RefSeq Alternation Syntax
- NM_000400.4:c.1381C>G
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2022-03-15
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002513097
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs