NM_144997.7(FLCN):c.34G>A (p.Glu12Lys) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 16, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004034377.1
Allele description [Variation Report for NM_144997.7(FLCN):c.34G>A (p.Glu12Lys)]
NM_144997.7(FLCN):c.34G>A (p.Glu12Lys)
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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Homo sapiens kinesin family member 3C, mRNA (cDNA clone MGC:102751 IMAGE:6504352...
Homo sapiens kinesin family member 3C, mRNA (cDNA clone MGC:102751 IMAGE:6504352), complete cdsgi|62531141|gb|BC092406.1|Nucleotide
-
Homo sapiens kinesin family member 3C, mRNA (cDNA clone MGC:164414 IMAGE:4014680...
Homo sapiens kinesin family member 3C, mRNA (cDNA clone MGC:164414 IMAGE:40146805), complete cdsgi|124376173|gb|BC132783.1|Nucleotide
-
Maxillofacial Osteoid Osteoma
Maxillofacial Osteoid OsteomaMedGen
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See more...Assertion and evidence details
Last Updated: Jun 9, 2024