NM_001048174.2(MUTYH):c.26G>A (p.Gly9Glu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 3, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000566677.3
Allele description [Variation Report for NM_001048174.2(MUTYH):c.26G>A (p.Gly9Glu)]
NM_001048174.2(MUTYH):c.26G>A (p.Gly9Glu)
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
-
UI-CF-EN1-adf-d-18-0-UI.s1 UI-CF-EN1 Homo sapiens cDNA clone UI-CF-EN1-adf-d-18-...
UI-CF-EN1-adf-d-18-0-UI.s1 UI-CF-EN1 Homo sapiens cDNA clone UI-CF-EN1-adf-d-18-0-UI 3', mRNA sequencegi|19603177|gnl|dbEST|11799368|gb|B 70.1|Nucleotide
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Last Updated: May 1, 2024