NM_000546.6(TP53):c.639A>G (p.Arg213=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Benign (4 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:
- RCV000162403.13
Allele description [Variation Report for NM_000546.6(TP53):c.639A>G (p.Arg213=)]
NM_000546.6(TP53):c.639A>G (p.Arg213=)
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
-
B4GALT5 [Taeniopygia guttata]
B4GALT5 [Taeniopygia guttata]Gene ID:100219705Gene
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See more...Assertion and evidence details
Last Updated: Jun 29, 2024