NM_000251.3(MSH2):c.816G>T (p.Ala272=) AND Lynch syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004002336.2
Allele description [Variation Report for NM_000251.3(MSH2):c.816G>T (p.Ala272=)]
NM_000251.3(MSH2):c.816G>T (p.Ala272=)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
-
conserved hypothetical protein [Shigella flexneri 5 str. 8401]
conserved hypothetical protein [Shigella flexneri 5 str. 8401]gi|110617533|gnl|mgcchina|SFV_4217| F06200.1|Protein
-
leucyl-tRNA synthetase [Pyrococcus furiosus DSM 3638]
leucyl-tRNA synthetase [Pyrococcus furiosus DSM 3638]gi|18892929|gb|AAL81014.1||gnl|UUGC 90.1Protein
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024