Annotation Detail
Information
- Associated Genes
- PRSS1 TRB
- Associated Variants
-
PRSS1 p.Asn29Ile (p.N29I)
(
ENST00000311737.12,
ENST00000486171.5,
ENST00000492062.2 )
PRSS1 p.Asn29Ile (p.N29I) ( ENST00000311737.12, ENST00000486171.5, ENST00000492062.2 ) - Associated Disease
- Trypsinogen deficiency Hereditary pancreatitis
- Source Database
- ClinVar
- Description
- NM_002769.5(PRSS1):c.86A>T (p.Asn29Ile) AND multiple conditions
- ClinVar Allele ID
- 26916
- ClinVar RefSeq Alternation Syntax
- NM_002769.5:c.86A>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2018-10-31
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000763166
- ClinVar Disease
- Trypsinogen deficiency
- ClinVar Disease
- Hereditary pancreatitis
- Observed Origin Sample
- unknown
Drugs