NM_000251.3(MSH2):c.1849G>C (p.Val617Leu) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 15, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000629939.7
Allele description [Variation Report for NM_000251.3(MSH2):c.1849G>C (p.Val617Leu)]
NM_000251.3(MSH2):c.1849G>C (p.Val617Leu)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
02q222 - Chromosomal Variation in Man
02q222 - Chromosomal Variation in Man
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Last Updated: Sep 29, 2024