NM_003073.5(SMARCB1):c.1062G>A (p.Glu354=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003348859.2
Allele description [Variation Report for NM_003073.5(SMARCB1):c.1062G>A (p.Glu354=)]
NM_003073.5(SMARCB1):c.1062G>A (p.Glu354=)
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
-
histone deacetylase 9 isoform 3 [Homo sapiens]
histone deacetylase 9 isoform 3 [Homo sapiens]gi|7662280|ref|NP_055522.1|Protein
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See more...Assertion and evidence details
Last Updated: May 1, 2024