Annotation Detail
Information
- Associated Genes
- PALLD
- Associated Variants
-
PALLD c.1964+44318A>G
(
ENST00000261509.10,
ENST00000505667.6,
ENST00000512127.5 )
PALLD c.1964+44318A>G ( ENST00000261509.10, ENST00000505667.6, ENST00000512127.5 ) - Associated Disease
- pancreatic adenocarcinoma
- Source Database
- ClinVar
- Description
- NM_001166108.2(PALLD):c.1964+44318A>G AND Pancreatic adenocarcinoma
- ClinVar Allele ID
- 1154706
- ClinVar RefSeq Alternation Syntax
- NM_001166109.2:c.818+44318A>G
- ClinVar RefSeq Alternation Syntax
- NM_001166108.2:c.1964+44318A>G
- ClinVar RefSeq Alternation Syntax
- NM_016081.4:c.1964+44318A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-29
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001510107
- ClinVar Disease
- Pancreatic adenocarcinoma
- Observed Origin Sample
- germline
Drugs