NM_000179.3(MSH6):c.2236T>C (p.Phe746Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002420672.2
Allele description [Variation Report for NM_000179.3(MSH6):c.2236T>C (p.Phe746Leu)]
NM_000179.3(MSH6):c.2236T>C (p.Phe746Leu)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
LGALS2 [Delphinapterus leucas]
LGALS2 [Delphinapterus leucas]Gene ID:111186388Gene
-
Synj1 synaptojanin 1 [Rattus norvegicus]
Synj1 synaptojanin 1 [Rattus norvegicus]Gene ID:85238Gene
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Last Updated: Sep 29, 2024