NM_000251.3(MSH2):c.198C>T (p.Tyr66=) AND Lynch syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 5, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003998489.2
Allele description [Variation Report for NM_000251.3(MSH2):c.198C>T (p.Tyr66=)]
NM_000251.3(MSH2):c.198C>T (p.Tyr66=)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
-
St8sia4 protein [Mus musculus]
St8sia4 protein [Mus musculus]gi|37805453|gb|AAH60112.1|Protein
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024