Annotation Detail
Information
- Associated Genes
- SLX4
- Associated Variants
-
SLX4 p.Pro929Leu (p.P929L)
(
ENST00000294008.4 )
SLX4 p.Pro929Leu (p.P929L) ( ENST00000294008.4 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_032444.4(SLX4):c.2786C>T (p.Pro929Leu) AND not provided
- ClinVar Allele ID
- 242418
- ClinVar RefSeq Alternation Syntax
- NM_032444.4:c.2786C>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001573902
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs