"Center of Medical Genetics and Primary Health Care"[submitter] AND "P - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 126740	NM_024675.4(PALB2):c.3428T>A (p.Leu1143His)	PALB2 (L1143H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 460986	NM_024675.4(PALB2):c.3299_3306dup (p.Val1103fs)	PALB2 (V1103fs)	Duplication (frameshift variant)	not provided +2 more	GPathogenic
Select item 460961	NM_024675.4(PALB2):c.2821A>G (p.Ile941Val)	PALB2 (I941V)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 126669	NM_024675.4(PALB2):c.2590C>T (p.Pro864Ser)	PALB2 (P864S)	Single nucleotide variant (missense variant)	not specified +7 more	GBenign/Likely benign
Select item 126630	NM_024675.4(PALB2):c.2014G>C (p.Glu672Gln)	PALB2 (E672Q)	Single nucleotide variant (missense variant)	Familial cancer of breast	GBenign FDA Recognized database
Select item 410166	NM_024675.4(PALB2):c.932_933insC (p.Lys311fs)	PALB2 (K311fs)	Insertion (frameshift variant)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic
Select item 134992	NM_024675.4(PALB2):c.833_834delinsAT (p.Leu278His)	PALB2 (L278H)	Indel (missense variant)	not provided +7 more	GConflicting classifications of pathogenicity

ClinVar