Annotation Detail
Information
- Associated Genes
- PSCA JRK
- Associated Variants
-
PSCA c.-26C>T
(
ENST00000301258.5,
ENST00000513264.1 )
PSCA c.-26C>T ( ENST00000301258.5, ENST00000513264.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_005672.5(PSCA):c.-26C>T AND not provided
- ClinVar Allele ID
- 692356
- ClinVar RefSeq Alternation Syntax
- NM_005672.5:c.-26C>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-07-02
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000874560
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs