NM_005591.4(MRE11):c.1497G>A (p.Glu499=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 23, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000167370.3
Allele description [Variation Report for NM_005591.4(MRE11):c.1497G>A (p.Glu499=)]
NM_005591.4(MRE11):c.1497G>A (p.Glu499=)
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
-
CECR5-AS1 (40)
MeSH
-
Homo sapiens beta-succinyl CoA synthetase mRNA, complete cds
Homo sapiens beta-succinyl CoA synthetase mRNA, complete cdsgi|33150621|gb|AF087890.1|Nucleotide
-
UI-E-EJ0-aif-c-14-0-UI.s1 UI-E-EJ0 Homo sapiens cDNA clone UI-E-EJ0-aif-c-14-0-U...
UI-E-EJ0-aif-c-14-0-UI.s1 UI-E-EJ0 Homo sapiens cDNA clone UI-E-EJ0-aif-c-14-0-UI 3', mRNA sequencegi|18988094|gnl|dbEST|11259131|gb|B 98.1|Nucleotide
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Last Updated: May 1, 2024