C3150547[trait identifier] AND "Institute of Human Genetics, Universit - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 128144	NM_024675.4(PALB2):c.3549C>A (p.Tyr1183Ter)	PALB2 (Y1183*)	Single nucleotide variant (nonsense)	Familial cancer of breast	GPathogenic FDA Recognized database
Select item 182771	NM_024675.4(PALB2):c.2834+1G>A	PALB2	Single nucleotide variant (splice donor variant)	not provided +5 more	GPathogenic/Likely pathogenic
Select item 126613	NM_024675.4(PALB2):c.1676A>G (p.Gln559Arg)	PALB2 (Q559R)	Single nucleotide variant (missense variant)	not provided +7 more	GBenign/Likely benign
Select item 128117	NM_024675.4(PALB2):c.1240C>T (p.Arg414Ter)	PALB2 (R414*)	Single nucleotide variant (nonsense)	Breast-ovarian cancer, familial, susceptibility to, 5 +7 more	GPathogenic
Select item 126768	NM_024675.4(PALB2):c.757_758del (p.Leu253fs)	PALB2 (L253fs)	Microsatellite (frameshift variant)	Familial cancer of breast +6 more	GPathogenic
Select item 126757	NM_024675.4(PALB2):c.509_510del (p.Arg170fs)	PALB2	Deletion (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 1 +10 more	GPathogenic
Select item 126623	NM_024675.4(PALB2):c.172_175del (p.Gln60fs)	PALB2 (Q60fs)	Microsatellite (frameshift variant)	not provided +5 more	GPathogenic/Likely pathogenic

ClinVar