Annotation Detail
Information
- Associated Genes
- ERCC2
- Associated Variants
-
ERCC2 p.Gly713Arg (p.G713R)
(
ENST00000391944.8,
ENST00000391945.10,
ENST00000684407.1 )
ERCC2 p.Gly713Arg (p.G713R) ( ENST00000391944.8, ENST00000391945.10, ENST00000684407.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000400.4(ERCC2):c.2137G>C (p.Gly713Arg) AND not specified
- ClinVar Allele ID
- 31825
- ClinVar RefSeq Alternation Syntax
- NM_000400.4:c.2137G>C
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-04-03
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003230368
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs