List of variants in gene BRIP1 reported as not provided by GenomeConnect - Invitae Patient Insights Network

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.2220G>T (p.Gln740His)	rs45589637	0.00041
NM_032043.3(BRIP1):c.3444C>A (p.Asp1148Glu)	rs28997573	0.00011
NM_032043.3(BRIP1):c.2392C>T (p.Arg798Ter)	rs137852986	0.00010
NM_032043.3(BRIP1):c.2469G>T (p.Arg823Ser)	rs587780239	0.00003
NM_032043.3(BRIP1):c.1054T>C (p.Tyr352His)	rs730881632	0.00001
NM_032043.3(BRIP1):c.1315C>T (p.Arg439Ter)	rs587780226	0.00001
NM_032043.3(BRIP1):c.2071A>C (p.Ile691Leu)	rs587782356	0.00001
NM_032043.3(BRIP1):c.3464G>A (p.Gly1155Glu)	rs45603843	0.00001
NM_032043.3(BRIP1):c.1853_1854insG (p.Pro619fs)	rs587781985
NM_032043.3(BRIP1):c.2684_2687del (p.Val894_Ser895insTer)	rs760551339
NM_032043.3(BRIP1):c.3374_3376del (p.Ala1125del)	rs745344948
NM_032043.3(BRIP1):c.500C>T (p.Thr167Ile)	rs758218234

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