NM_000179.3(MSH6):c.1028C>A (p.Pro343His) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 11, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001524238.2
Allele description [Variation Report for NM_000179.3(MSH6):c.1028C>A (p.Pro343His)]
NM_000179.3(MSH6):c.1028C>A (p.Pro343His)
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
-
ubiquitin-specific protease 17 [Arabidopsis thaliana]
ubiquitin-specific protease 17 [Arabidopsis thaliana]gi|15238468|ref|NP_201348.1|Protein
-
CRYBG3 [Propithecus coquereli]
CRYBG3 [Propithecus coquereli]Gene ID:105817166Gene
-
PPP1R3A [Propithecus coquereli]
PPP1R3A [Propithecus coquereli]Gene ID:105817140Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024