ClinVar for PMC (Select 4106182) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 185111	NM_007294.4(BRCA1):c.2773A>G (p.Ile925Val)	BRCA1 (I925V +20 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 54935	NM_007294.4(BRCA1):c.3608G>A (p.Arg1203Gln)	BRCA1, LOC126862571 (R1203Q +21 more)	Single nucleotide variant (intron variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GBenign
Select item 54777	NM_007294.4(BRCA1):c.3143G>T (p.Gly1048Val)	BRCA1 (G1048V +20 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GBenign
Select item 54776	NM_007294.4(BRCA1):c.3143G>A (p.Gly1048Asp)	BRCA1 (G1048D +20 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 54338	NM_007294.4(BRCA1):c.1733C>A (p.Ser578Tyr)	BRCA1 (S578Y +20 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 37489	NM_007294.4(BRCA1):c.2773A>C (p.Ile925Leu)	BRCA1 (I925L +20 more)	Single nucleotide variant (intron variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GBenign

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