NM_001048174.2(MUTYH):c.1476A>G (p.Lys492=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 19, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001012180.3
Allele description [Variation Report for NM_001048174.2(MUTYH):c.1476A>G (p.Lys492=)]
NM_001048174.2(MUTYH):c.1476A>G (p.Lys492=)
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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602043351F1 NCI_CGAP_Brn67 Homo sapiens cDNA clone IMAGE:4180981 5', mRNA sequen...
602043351F1 NCI_CGAP_Brn67 Homo sapiens cDNA clone IMAGE:4180981 5', mRNA sequencegi|11616251|gnl|dbEST|6965285|gb|BF 8.1|Nucleotide
-
UI-E-CI1-afp-f-12-0-UI.s1 UI-E-CI1 Homo sapiens cDNA clone UI-E-CI1-afp-f-12-0-U...
UI-E-CI1-afp-f-12-0-UI.s1 UI-E-CI1 Homo sapiens cDNA clone UI-E-CI1-afp-f-12-0-UI 3', mRNA sequencegi|23654536|gnl|dbEST|14195139|gb|B 42.1|Nucleotide
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Last Updated: Sep 29, 2024