List of variants in gene BRIP1 reported as pathogenic for Breast and/or ovarian cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.2392C>T (p.Arg798Ter)	rs137852986	0.00010
NM_032043.3(BRIP1):c.-206_94-576delinsCTAAAAATCCAAAATTAGCTGGGCGTGGTGGCGCA
NM_032043.3(BRIP1):c.1049del (p.Cys350fs)	rs2077989420
NM_032043.3(BRIP1):c.128_131del (p.Leu43fs)	rs1064794202
NM_032043.3(BRIP1):c.1889del (p.Thr630fs)	rs1064793626
NM_032043.3(BRIP1):c.1_2del (p.Met1fs)	rs876661246
NM_032043.3(BRIP1):c.2038_2039dup (p.Leu680fs)	rs587778134
NM_032043.3(BRIP1):c.2400C>G (p.Tyr800Ter)	rs574552037
NM_032043.3(BRIP1):c.2684_2687del (p.Val894_Ser895insTer)	rs760551339

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