Annotation Detail
Information
- Associated Genes
- WNT10A
- Associated Variants
-
WNT10A p.Gly213Ser (p.G213S)
(
ENST00000258411.8 )
WNT10A p.Gly213Ser (p.G213S) ( ENST00000258411.8 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_025216.3(WNT10A):c.637G>A (p.Gly213Ser) AND not provided
- ClinVar Allele ID
- 143206
- ClinVar RefSeq Alternation Syntax
- NM_025216.3:c.637G>A
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2022-12-20
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001555273
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs