NM_000251.3(MSH2):c.198C>T (p.Tyr66=) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000206199.14
Allele description
NM_000251.3(MSH2):c.198C>T (p.Tyr66=)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
Homo sapiens plakophilin 2 (PKP2), transcript variant 2a, mRNA
Homo sapiens plakophilin 2 (PKP2), transcript variant 2a, mRNAgi|1779260915|ref|NM_001005242.3|Nucleotide
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Last Updated: Sep 16, 2024