NM_001048174.2(MUTYH):c.1239G>A (p.Glu413=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Jun 23, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000131785.12
Allele description [Variation Report for NM_001048174.2(MUTYH):c.1239G>A (p.Glu413=)]
NM_001048174.2(MUTYH):c.1239G>A (p.Glu413=)
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
-
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Last Updated: May 1, 2024