List of variants in gene BRIP1 reported as uncertain significance 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: 31

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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.1255C>T (p.Arg419Trp)	rs150624408	0.00026
NM_032043.3(BRIP1):c.139C>G (p.Pro47Ala)	rs28903098	0.00024
NM_032043.3(BRIP1):c.854A>G (p.His285Arg)	rs141055990	0.00017
NM_032043.3(BRIP1):c.2440C>T (p.Arg814Cys)	rs201869624	0.00016
NM_032043.3(BRIP1):c.2087C>T (p.Pro696Leu)	rs147755155	0.00006
NM_032043.3(BRIP1):c.3103C>T (p.Arg1035Cys)	rs45437094	0.00006
NM_032043.3(BRIP1):c.550G>T (p.Asp184Tyr)	rs201047375	0.00006
NM_032043.3(BRIP1):c.415T>G (p.Ser139Ala)	rs202072866	0.00004
NM_032043.3(BRIP1):c.2469G>T (p.Arg823Ser)	rs587780239	0.00003
NM_032043.3(BRIP1):c.2492+2dup	rs587780240	0.00003
NM_032043.3(BRIP1):c.3064G>A (p.Glu1022Lys)	rs587782808	0.00002
NM_032043.3(BRIP1):c.3331G>C (p.Glu1111Gln)	rs587780248	0.00002
NM_032043.3(BRIP1):c.386C>T (p.Pro129Leu)	rs587780831	0.00002
NM_032043.3(BRIP1):c.10A>G (p.Met4Val)	rs45512093	0.00001
NM_032043.3(BRIP1):c.1187A>G (p.His396Arg)	rs996493095	0.00001
NM_032043.3(BRIP1):c.2441G>A (p.Arg814His)	rs45468199	0.00001
NM_032043.3(BRIP1):c.2579T>C (p.Leu860Pro)	rs587780242	0.00001
NM_032043.3(BRIP1):c.2802T>G (p.Phe934Leu)	rs1259968679	0.00001
NM_032043.3(BRIP1):c.3262C>T (p.His1088Tyr)	rs878855154	0.00001
NM_032043.3(BRIP1):c.1090A>G (p.Ile364Val)	rs770306753
NM_032043.3(BRIP1):c.1141-9A>G	rs1555607258
NM_032043.3(BRIP1):c.1180G>C (p.Glu394Gln)	rs2077952602
NM_032043.3(BRIP1):c.1715T>G (p.Val572Gly)	rs1603334516
NM_032043.3(BRIP1):c.2097+5G>A	rs1567808616
NM_032043.3(BRIP1):c.256TGT[2] (p.Cys88del)	rs587781388
NM_032043.3(BRIP1):c.3020C>A (p.Ser1007Tyr)	rs886053214
NM_032043.3(BRIP1):c.3374_3376del (p.Ala1125del)	rs745344948
NM_032043.3(BRIP1):c.3409T>C (p.Tyr1137His)	rs2061308195
NM_032043.3(BRIP1):c.613T>G (p.Phe205Val)	rs1603361561
NM_032043.3(BRIP1):c.819G>T (p.Met273Ile)	rs2145415194

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