NM_000251.3(MSH2):c.2262_2267del (p.Ser755_Thr756del) AND Lynch syndrome 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 26, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003990397.2
Allele description [Variation Report for NM_000251.3(MSH2):c.2262_2267del (p.Ser755_Thr756del)]
NM_000251.3(MSH2):c.2262_2267del (p.Ser755_Thr756del)
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: Aug 4, 2024