ClinVar (all) for Orgtrack (Select 506119) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 403704	NM_000059.4(BRCA2):c.-39-1G>A	BRCA2	Single nucleotide variant (splice acceptor variant +1 more)	Familial cancer of breast	GLikely pathogenic
Select item 128209	NM_058216.3(RAD51C):c.706-2A>G	RAD51C	Single nucleotide variant (splice acceptor variant)	RAD51C-related condition +5 more	GPathogenic/Likely pathogenic
Select item 128201	NM_058216.3(RAD51C):c.1026+5_1026+7del	RAD51C	Deletion (intron variant)	Hereditary cancer-predisposing syndrome +5 more	GPathogenic/Likely pathogenic
Select item 126018	NM_000059.3(BRCA2):c.156_157insAlu	BRCA2	Insertion	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 51710	NM_000059.4(BRCA2):c.475+3A>G	BRCA2	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 38242	NM_000059.4(BRCA2):c.9501+3A>T	BRCA2	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 38130	NM_000059.4(BRCA2):c.7975A>G (p.Arg2659Gly)	BRCA2 (R2659G)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 37605	NM_007294.4(BRCA1):c.4675G>C (p.Glu1559Gln)	BRCA1 (E1559Q +75 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GPathogenic/Likely pathogenic

ClinVar