NM_024675.4(PALB2):c.2074C>T (p.Gln692Ter) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Pathogenic (2 submissions)
- Last evaluated:
- Nov 18, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000562385.7
Allele description [Variation Report for NM_024675.4(PALB2):c.2074C>T (p.Gln692Ter)]
NM_024675.4(PALB2):c.2074C>T (p.Gln692Ter)
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
-
Synthetic construct Homo sapiens clone IMAGE:100068984, MGC:198995 olfactory rec...
Synthetic construct Homo sapiens clone IMAGE:100068984, MGC:198995 olfactory receptor, family 5, subfamily L, member 2 (OR5L2) mRNA, encodes complete proteingi|225000733|gb|BC172290.1|Nucleotide
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Last Updated: Sep 29, 2024