NM_000251.3(MSH2):c.1389G>T (p.Val463=) AND Lynch syndrome 1
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 28, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000986671.8
Allele description [Variation Report for NM_000251.3(MSH2):c.1389G>T (p.Val463=)]
NM_000251.3(MSH2):c.1389G>T (p.Val463=)
Condition(s)
- Name:
- Lynch syndrome 1
- Synonyms:
- COLON CANCER, FAMILIAL NONPOLYPOSIS, TYPE 1; MSH2-Related Hereditary Non-Polyposis Colon Cancer; Lynch syndrome I; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0007356; MedGen: C2936783; Orphanet: 144; OMIM: 120435
Assertion and evidence details
Last Updated: Oct 20, 2024