NM_024675.4(PALB2):c.3059A>T (p.Gln1020Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jul 7, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001805471.4
Allele description [Variation Report for NM_024675.4(PALB2):c.3059A>T (p.Gln1020Leu)]
NM_024675.4(PALB2):c.3059A>T (p.Gln1020Leu)
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
-
DNA-damage-inducible transcript 4 [Rattus norvegicus]
DNA-damage-inducible transcript 4 [Rattus norvegicus]gi|149038775|gb|EDL93064.1||gnl|WGS |rCP24701Protein
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See more...Assertion and evidence details
Last Updated: May 1, 2024