"CZECANCA consortium"[submitter] AND "PALB2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 530199	NM_024675.4(PALB2):c.3494C>A (p.Ser1165Ter)	PALB2 (S1165*)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic/Likely pathogenic
Select item 989424	NM_024675.4(PALB2):c.1193_1194del (p.Val398fs)	PALB2 (V398fs)	Deletion (frameshift variant)	Breast and/or ovarian cancer	GPathogenic
Select item 632930	NM_024675.4(PALB2):c.761C>G (p.Ser254Ter)	PALB2 (S254*)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic/Likely pathogenic
Select item 126764	NM_024675.4(PALB2):c.697del (p.Val233fs)	PALB2 (V233fs)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic
Select item 141372	NM_024675.4(PALB2):c.654del (p.Asp219fs)	PALB2 (D219fs)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic
Select item 126757	NM_024675.4(PALB2):c.509_510del (p.Arg170fs)	PALB2	Deletion (frameshift variant)	Malignant tumor of breast +11 more	GPathogenic
Select item 126623	NM_024675.4(PALB2):c.172_175del (p.Gln60fs)	DCTN5, PALB2 (Q60fs)	Microsatellite (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 5 +6 more	GPathogenic/Likely pathogenic

ClinVar