NM_000546.6(TP53):c.657C>A (p.Pro219=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jun 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000164354.3
Allele description [Variation Report for NM_000546.6(TP53):c.657C>A (p.Pro219=)]
NM_000546.6(TP53):c.657C>A (p.Pro219=)
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
-
RecName: Full=Testis-specific Y-encoded-like protein 1; Short=TSPY-like protein ...
RecName: Full=Testis-specific Y-encoded-like protein 1; Short=TSPY-like protein 1gi|209572711|sp|Q9H0U9.3|TSYL1_HUMAProtein
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See more...Assertion and evidence details
Last Updated: Feb 20, 2024