NM_000251.3(MSH2):c.1095T>C (p.Ala365=) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 2, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001424783.15
Allele description [Variation Report for NM_000251.3(MSH2):c.1095T>C (p.Ala365=)]
NM_000251.3(MSH2):c.1095T>C (p.Ala365=)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
Homo sapiens lecithin-cholesterol acyltransferase (LCAT), mRNA
Homo sapiens lecithin-cholesterol acyltransferase (LCAT), mRNAgi|1653962002|ref|NM_000229.2|Nucleotide
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Last Updated: Oct 13, 2024