NM_000546.6(TP53):c.762C>T (p.Ile254=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 28, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001184847.2
Allele description [Variation Report for NM_000546.6(TP53):c.762C>T (p.Ile254=)]
NM_000546.6(TP53):c.762C>T (p.Ile254=)
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
-
C-terminal-binding protein 2 isoform X1 [Dermochelys coriacea]
C-terminal-binding protein 2 isoform X1 [Dermochelys coriacea]gi|1950473180|ref|XP_038269836.1|Protein
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023