NM_001166108.2(PALLD):c.2393T>C (p.Met798Thr) AND Pancreatic cancer, susceptibility to, 1
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000365201.12
Allele description [Variation Report for NM_001166108.2(PALLD):c.2393T>C (p.Met798Thr)]
NM_001166108.2(PALLD):c.2393T>C (p.Met798Thr)
Condition(s)
Assertion and evidence details
Last Updated: Nov 3, 2024