List of variants in gene BRIP1 reported as likely benign for Malignant tumor of breast

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.517C>T (p.Arg173Cys)	rs4988345	0.00363
NM_032043.3(BRIP1):c.2937A>G (p.Lys979=)	rs75091137	0.00194
NM_032043.3(BRIP1):c.2286T>C (p.Arg762=)	rs61754141	0.00173
NM_032043.3(BRIP1):c.890A>G (p.Lys297Arg)	rs28997570	0.00113
NM_032043.3(BRIP1):c.790C>T (p.Arg264Trp)	rs28997569	0.00104
NM_032043.3(BRIP1):c.3378A>C (p.Glu1126Asp)	rs145855459	0.00076
NM_032043.3(BRIP1):c.587A>G (p.Asn196Ser)	rs550707862	0.00017
NM_032043.3(BRIP1):c.69G>A (p.Pro23=)	rs45458996	0.00004
NM_032043.3(BRIP1):c.2748C>T (p.Tyr916=)	rs555200296	0.00003
NM_032043.3(BRIP1):c.702G>A (p.Lys234=)	rs45512798	0.00003
NM_032043.3(BRIP1):c.*15C>G	rs1057523100
NM_032043.3(BRIP1):c.1170C>T (p.Val390=)	rs754755989
NM_032043.3(BRIP1):c.1566A>G (p.Ser522=)	rs985465808
NM_032043.3(BRIP1):c.2158G>A (p.Val720Met)	rs1555591459

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