NM_024675.4(PALB2):c.3086C>T (p.Thr1029Ile) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 6, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003160502.2
Allele description [Variation Report for NM_024675.4(PALB2):c.3086C>T (p.Thr1029Ile)]
NM_024675.4(PALB2):c.3086C>T (p.Thr1029Ile)
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
-
E3 ubiquitin-protein ligase HEL2 [Saccharomyces cerevisiae S288C]
E3 ubiquitin-protein ligase HEL2 [Saccharomyces cerevisiae S288C]gi|398366351|ref|NP_010552.3|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024