Annotation Detail
Information
- Associated Genes
- CARTPT
- Associated Variants
-
CARTPT c.159+172C>T
(
ENST00000296777.5 )
CARTPT c.159+172C>T ( ENST00000296777.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_004291.4(CARTPT):c.159+172C>T AND not provided
- ClinVar Allele ID
- 1238760
- ClinVar RefSeq Alternation Syntax
- NM_004291.4:c.159+172C>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-11-10
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001655304
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs