NM_000251.3(MSH2):c.1857T>G (p.Tyr619Ter) AND Lynch syndrome
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Sep 5, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000076303.4
Allele description [Variation Report for NM_000251.3(MSH2):c.1857T>G (p.Tyr619Ter)]
NM_000251.3(MSH2):c.1857T>G (p.Tyr619Ter)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
-
S41 family peptidase [Leeuwenhoekiella palythoae]
S41 family peptidase [Leeuwenhoekiella palythoae]gi|2106384162|gnl|PRJNA766805|LDL79 5|gb|UBZ11621.1|Protein
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Last Updated: Sep 29, 2024