NM_000546.6(TP53):c.1064C>T (p.Ala355Val) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Conflicting interpretations of pathogenicity (3 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:
- RCV001009801.9
Allele description [Variation Report for NM_000546.6(TP53):c.1064C>T (p.Ala355Val)]
NM_000546.6(TP53):c.1064C>T (p.Ala355Val)
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
-
Rattus norvegicus phosphoribosyl transferase domain containing 1 (Prtfdc1), mRNA
Rattus norvegicus phosphoribosyl transferase domain containing 1 (Prtfdc1), mRNAgi|157817281|ref|NM_001106127.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024