Annotation Detail
Information
- Associated Genes
- PRSS1 TRB
- Associated Variants
-
PRSS1 p.Ala16Val (p.A16V)
(
ENST00000311737.12,
ENST00000486171.5,
ENST00000492062.2 )
PRSS1 p.Ala16Val (p.A16V) ( ENST00000311737.12, ENST00000486171.5, ENST00000492062.2 ) - Associated Disease
- Hereditary pancreatitis
- Source Database
- ClinVar
- Description
- NM_002769.5(PRSS1):c.47C>T (p.Ala16Val) AND Hereditary pancreatitis
- ClinVar Allele ID
- 46925
- ClinVar RefSeq Alternation Syntax
- NM_002769.5:c.47C>T
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2024-01-18
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000031920
- ClinVar Disease
- Hereditary pancreatitis
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs