NM_000179.3(MSH6):c.3689C>T (p.Ala1230Val) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jul 31, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002457452.3
Allele description [Variation Report for NM_000179.3(MSH6):c.3689C>T (p.Ala1230Val)]
NM_000179.3(MSH6):c.3689C>T (p.Ala1230Val)
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: May 1, 2024