Variant Term Annotation Report - Rat Genome Database

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VARIANT - TERM ANNOTATION REPORT

RGD ID:	8591413
Species:	Homo sapiens
RGD Object:	Variant
Symbol:	CV132188
Name:	NM_024675.4(PALB2):c.2749-18C>T

Acc ID:	DOID:9007071
Term:	Hereditary Neoplastic Syndromes
Definition:	The condition of a pattern of malignancies within a family, but not every individual's necessarily having the same neoplasm. Characteristically the tumor tends to occur at an earlier than average age, individuals may have more than one primary tumor, the tumors may be multicentric, usually more than 25 percent of the individuals in direct lineal descent from the proband are affected, and the cancer predisposition in these families behaves as an autosomal dominant trait with about 60 percent penetrance.
Definition Source(s):	MESH:D009386

Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.

Object Symbol	Qualifier	Evidence	With	Reference	Source	Notes	Original Reference(s)
CV132188		IAGP		8554872	ClinVar	ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome	PMID:22241545 PMID:25085752 PMID:25356972 PMID:25741868 PMID:28492532

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