Annotation Detail
Information
- Associated Genes
- U2AF1
- Associated Variants
-
U2AF1 p.Ser34Phe (p.S34F)
(
ENST00000291552.9,
ENST00000380276.6,
ENST00000459639.5 )
U2AF1 p.Ser34Phe (p.S34F) ( ENST00000291552.9, ENST00000380276.6, ENST00000459639.5 ) - Associated Disease
- pancreatic adenocarcinoma
- Source Database
- ClinVar
- Description
- NM_006758.3(U2AF1):c.101C>T (p.Ser34Phe) AND Pancreatic adenocarcinoma
- ClinVar Allele ID
- 362904
- ClinVar RefSeq Alternation Syntax
- NM_006758.3:c.101C>T
- ClinVar RefSeq Alternation Syntax
- NM_001025204.2:c.-186C>T
- ClinVar RefSeq Alternation Syntax
- NM_001025203.1:c.101C>T
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2016-05-31
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000418032
- ClinVar Disease
- Pancreatic adenocarcinoma
- Observed Origin Sample
- somatic
Drugs