List of variants in gene BRIP1 reported as likely benign by Mendelics

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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: 34

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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.577G>A (p.Val193Ile)	rs4988346	0.00305
NM_032043.3(BRIP1):c.2097+7G>A	rs4988352	0.00271
NM_032043.3(BRIP1):c.584T>C (p.Leu195Pro)	rs4988347	0.00197
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.195A>G (p.Gln65=)	rs141436143	0.00076
NM_032043.3(BRIP1):c.3378A>C (p.Glu1126Asp)	rs145855459	0.00076
NM_032043.3(BRIP1):c.3459T>C (p.Asp1153=)	rs4987050	0.00069
NM_032043.3(BRIP1):c.2220G>T (p.Gln740His)	rs45589637	0.00041
NM_032043.3(BRIP1):c.-30-3T>C	rs370728413	0.00014
NM_032043.3(BRIP1):c.2232C>T (p.Asp744=)	rs374362388	0.00006
NM_032043.3(BRIP1):c.3567T>C (p.Asp1189=)	rs764848326	0.00005
NM_032043.3(BRIP1):c.2100A>G (p.Leu700=)	rs766047812	0.00003
NM_032043.3(BRIP1):c.702G>A (p.Lys234=)	rs45512798	0.00003
NM_032043.3(BRIP1):c.728T>C (p.Ile243Thr)	rs587781860	0.00003
NM_032043.3(BRIP1):c.-95G>A	rs892920553	0.00002
NM_032043.2(BRIP1):c.2097+8A>C	rs730881642	0.00001
NM_032043.3(BRIP1):c.-225G>A	rs1603369188	0.00001
NM_032043.3(BRIP1):c.-56C>G	rs1054876315	0.00001
NM_032043.3(BRIP1):c.1455T>C (p.Ala485=)	rs773489367	0.00001
NM_032043.3(BRIP1):c.3122T>C (p.Met1041Thr)	rs761225576	0.00001
NM_032043.3(BRIP1):c.-165A>G	rs1603369145
NM_032043.3(BRIP1):c.1932A>T (p.Ser644=)	rs1603332998
NM_032043.3(BRIP1):c.1935+8G>T	rs767048212
NM_032043.3(BRIP1):c.2098-8C>T	rs917048033
NM_032043.3(BRIP1):c.2181A>G (p.Pro727=)	rs1603304559
NM_032043.3(BRIP1):c.2379+7C>T	rs1057520464
NM_032043.3(BRIP1):c.2905+31T>C	rs1603276473
NM_032043.3(BRIP1):c.3651G>T (p.Trp1217Cys)	rs542698396
NM_032043.3(BRIP1):c.380-6T>C	rs780921390
NM_032043.3(BRIP1):c.408A>C (p.Ala136=)	rs876660891
NM_032043.3(BRIP1):c.507+9_507+10del	rs747185394
NM_032043.3(BRIP1):c.588C>G (p.Asn196Lys)	rs758851721

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