NM_001349798.2(FBXW7):c.1513C>A (p.Arg505Ser) AND Carcinoma of esophagus
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- May 31, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000431685.2
Allele description [Variation Report for NM_001349798.2(FBXW7):c.1513C>A (p.Arg505Ser)]
NM_001349798.2(FBXW7):c.1513C>A (p.Arg505Ser)
Condition(s)
- Name:
- Carcinoma of esophagus
- Synonyms:
- Oesophageal carcinoma; Esophageal carcinoma
- Identifiers:
- MONDO: MONDO:0019086; MedGen: C0152018; Orphanet: 70482; Human Phenotype Ontology: HP:0011459
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Last Updated: Sep 16, 2024