NM_024675.4(PALB2):c.3307G>A (p.Val1103Met) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Conflicting interpretations of pathogenicity (3 submissions)
- Last evaluated:
- Nov 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000116103.16
Allele description [Variation Report for NM_024675.4(PALB2):c.3307G>A (p.Val1103Met)]
NM_024675.4(PALB2):c.3307G>A (p.Val1103Met)
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
-
33924[uid] (0)
Protein Family Models
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Last Updated: Oct 13, 2024