List of variants in gene BRIP1 reported as likely pathogenic for Neoplasm of ovary

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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: 10

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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.1240C>T (p.Gln414Ter)	rs368796923	0.00001
NM_032043.3(BRIP1):c.206-2A>G	rs786203700	0.00001
NM_032043.3(BRIP1):c.1853_1854insG (p.Pro619fs)	rs587781985
NM_032043.3(BRIP1):c.2038_2039dup (p.Leu680fs)	rs587778134
NM_032043.3(BRIP1):c.205+1del	rs1057517648
NM_032043.3(BRIP1):c.2111T>A (p.Leu704Ter)	rs1057517643
NM_032043.3(BRIP1):c.2379G>T (p.Gln793His)	rs1567779336
NM_032043.3(BRIP1):c.290_293del (p.Asn97fs)	rs763009188
NM_032043.3(BRIP1):c.2990_2993del (p.Thr997fs)	rs771028677

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